المؤلفون: Mirabdolhosseini SM; Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Centre, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Rejali L; Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Centre, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Yaghoob Taleghani M; Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Centre, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Sadeghi H; Genomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Kashfi SMH; Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Centre, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Behboudi Farahbakhsh F; Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Centre, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Golmohammadi M; Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Centre, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Larki P; Genomic Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Fatemi N; Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Centre, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Ketabi Moghadam P; Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Centre, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Nazemalhosseini Mojarad E; Gastroenterology and Liver Diseases Research Centre, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Sadeghi A; Gastroenterology and Liver Diseases Research Centre, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Asadzadeh Aghdaie H; Basic and Molecular Epidemiology of Gastrointestinal Disorders Research Centre, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran., Zali MR; Gastroenterology and Liver Diseases Research Centre, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

المصدر: Nucleosides, nucleotides & nucleic acids [Nucleosides Nucleotides Nucleic Acids] 2024; Vol. 43 (1), pp. 40-56. Date of Electronic Publication: 2023 Jul 05.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Taylor & Francis Country of Publication: United States NLM ID: 100892832 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-2335 (Electronic) Linking ISSN: 15257770 NLM ISO Abbreviation: Nucleosides Nucleotides Nucleic Acids Subsets: MEDLINE

مواضيع طبية MeSH: Genes, APC* , Adenomatous Polyposis Coli*/genetics , Adenomatous Polyposis Coli*/diagnosis , Adenomatous Polyposis Coli*/pathology, Humans ; Iran ; Germ-Line Mutation ; Phenotype

المؤلفون: Mori Y; Department of Digestive Tract and General Surgery, Saitama Medical Center, Saitama Medical University, 1981 Kamoda, Kawagoe, Saitama, 350-8550, Japan., Ishida H; Department of Digestive Tract and General Surgery, Saitama Medical Center, Saitama Medical University, 1981 Kamoda, Kawagoe, Saitama, 350-8550, Japan.; The Committee of Hereditary Colorectal Cancer, Japanese Society for Cancer of the Colon and Rectum, Tokyo, Japan., Chika N; Department of Digestive Tract and General Surgery, Saitama Medical Center, Saitama Medical University, 1981 Kamoda, Kawagoe, Saitama, 350-8550, Japan., Ito T; Department of Digestive Tract and General Surgery, Saitama Medical Center, Saitama Medical University, 1981 Kamoda, Kawagoe, Saitama, 350-8550, Japan., Amano K; Department of Digestive Tract and General Surgery, Saitama Medical Center, Saitama Medical University, 1981 Kamoda, Kawagoe, Saitama, 350-8550, Japan., Chikatani K; Department of Digestive Tract and General Surgery, Saitama Medical Center, Saitama Medical University, 1981 Kamoda, Kawagoe, Saitama, 350-8550, Japan., Takeuchi Y; The Committee of Hereditary Colorectal Cancer, Japanese Society for Cancer of the Colon and Rectum, Tokyo, Japan.; Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan., Kono M; Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan., Shichijo S; Department of Gastrointestinal Oncology, Osaka International Cancer Institute, Osaka, Japan., Chino A; The Committee of Hereditary Colorectal Cancer, Japanese Society for Cancer of the Colon and Rectum, Tokyo, Japan.; Department of Gastroenterology, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan., Nagasaki T; The Committee of Hereditary Colorectal Cancer, Japanese Society for Cancer of the Colon and Rectum, Tokyo, Japan.; Department of Gastroenterology, Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan., Takao A; The Committee of Hereditary Colorectal Cancer, Japanese Society for Cancer of the Colon and Rectum, Tokyo, Japan.; Department of Gastroenterology, Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital, Tokyo, Japan., Takao M; Department of Surgery, Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital, Tokyo, Japan., Nakamori S; Department of Surgery, Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital, Tokyo, Japan., Sasaki K; The Committee of Hereditary Colorectal Cancer, Japanese Society for Cancer of the Colon and Rectum, Tokyo, Japan.; Department of Surgical Oncology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan., Akagi K; The Committee of Hereditary Colorectal Cancer, Japanese Society for Cancer of the Colon and Rectum, Tokyo, Japan.; Department of Molecular Diagnosis and Cancer Prevention, Saitama Cancer Center, Saitama, Japan., Yamaguchi T; The Committee of Hereditary Colorectal Cancer, Japanese Society for Cancer of the Colon and Rectum, Tokyo, Japan. tatsuro@yamaguchi.email.ne.jp.; Department of Clinical Genetics, Tokyo Metropolitan Cancer and Infectious Diseases Center, Komagome Hospital, 3-18-22, Bunkyo-ku, Honkomagome, Tokyo, 113-8677, Japan. tatsuro@yamaguchi.email.ne.jp., Tanakaya K; The Committee of Hereditary Colorectal Cancer, Japanese Society for Cancer of the Colon and Rectum, Tokyo, Japan.; Department of Surgery, National Hospital Organization Iwakuni Clinical Center, Iwakuni, Japan., Naohiro T; The Committee of Hereditary Colorectal Cancer, Japanese Society for Cancer of the Colon and Rectum, Tokyo, Japan.; Department of Surgery, Toyonaka Municipal Hospital, Toyonaka, Japan., Ajioka Y; The Committee of Hereditary Colorectal Cancer, Japanese Society for Cancer of the Colon and Rectum, Tokyo, Japan.; Division of Molecular and Diagnostic Pathology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.

المصدر: International journal of clinical oncology [Int J Clin Oncol] 2023 Dec; Vol. 28 (12), pp. 1641-1650. Date of Electronic Publication: 2023 Oct 18.

نوع المنشور: Multicenter Study; Journal Article

بيانات الدورية: Publisher: Springer-Verlag Tokyo Country of Publication: Japan NLM ID: 9616295 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1437-7772 (Electronic) Linking ISSN: 13419625 NLM ISO Abbreviation: Int J Clin Oncol Subsets: MEDLINE

مواضيع طبية MeSH: Genes, APC* , Adenomatous Polyposis Coli*/genetics , Adenomatous Polyposis Coli*/surgery , Adenomatous Polyposis Coli*/pathology, Male ; Humans ; Female ; Middle Aged ; Genotype ; Prospective Studies ; Retrospective Studies

المؤلفون: Privitera F; Laboratory of Clinical Molecular Genetics and Cytogenetics, IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy., Piccini F; Laboratory of Clinical Molecular Genetics and Cytogenetics, IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy., Recalcati MP; Laboratory of Clinical Molecular Genetics and Cytogenetics, IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy., Presi S; Laboratory of Clinical Molecular Genetics and Cytogenetics, IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy., Mazzola S; Medical Genetics, ASST del Garda, Desenzano, 25015 Brescia, Italy., Carrera P; Laboratory of Clinical Molecular Genetics and Cytogenetics, IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy.; Unit of Genomics for Diagnosis of Human Diseases, IRCCS San Raffaele Scientific Institute, 20132 Milan, Italy.

المصدر: Genes [Genes (Basel)] 2023 Jul 23; Vol. 14 (7). Date of Electronic Publication: 2023 Jul 23.

نوع المنشور: Review; Case Reports; Journal Article

بيانات الدورية: Publisher: MDPI Country of Publication: Switzerland NLM ID: 101551097 Publication Model: Electronic Cited Medium: Internet ISSN: 2073-4425 (Electronic) Linking ISSN: 20734425 NLM ISO Abbreviation: Genes (Basel) Subsets: MEDLINE

مواضيع طبية MeSH: Chromosome Deletion* , Intellectual Disability*/genetics , Genes, APC* , Adenomatous Polyposis Coli Protein*/genetics, Humans ; Chromosome Aberrations ; Phenotype

SCR Disease Name: Chromosome 5q Deletion Syndrome

المؤلفون: Komeda Y; Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Japan., Ishikawa H; Department of Molecular-Targeting Prevention, Kyoto Prefectural University of Medicine, Japan., Yoshida T; Department of Genetic Medicine and Services, National Cancer Center Hospital, Japan.; Department of Clinical Genomics, National Cancer Center Research Institute, Japan., Ushiama M; Department of Genetic Medicine and Services, National Cancer Center Hospital, Japan.; Department of Clinical Genomics, National Cancer Center Research Institute, Japan., Yoshida S; Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Japan., Nomura K; Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Japan., Kono M; Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Japan., Omoto S; Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Japan., Takenaka M; Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Japan., Hagiwara S; Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Japan., Kashida H; Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Japan., Kudo M; Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Japan.

المصدر: Internal medicine (Tokyo, Japan) [Intern Med] 2024 Apr 15; Vol. 63 (8), pp. 1075-1079. Date of Electronic Publication: 2023 Aug 09.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Japanese Society of Internal Medicine Country of Publication: Japan NLM ID: 9204241 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1349-7235 (Electronic) Linking ISSN: 09182918 NLM ISO Abbreviation: Intern Med Subsets: MEDLINE

مواضيع طبية MeSH: Adenomatous Polyposis Coli*/genetics , Duodenal Neoplasms*, Female ; Humans ; Adolescent ; Genes, APC ; Germ-Line Mutation/genetics ; Phenotype

المؤلفون: Oliveira D; Medical Genetics Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal; University Clinic of Genetics, Faculty of Medicine, Universidade de Coimbra, Coimbra, Portugal; Clinical Academic Center of Coimbra, Coimbra, Portugal. Electronic address: danielaoliveira@ulscoimbra.min-saude.pt., Maia S; Medical Genetics Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal; University Clinic of Genetics, Faculty of Medicine, Universidade de Coimbra, Coimbra, Portugal; Clinical Academic Center of Coimbra, Coimbra, Portugal., Balacó I; Paediatric Ortopedic Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal., Coelho P; Radiology Department, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal., Almeida S; Paediatric Gastroenterology Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal., Venâncio M; Medical Genetics Unit, Hospital Dona Estefânia, Centro Hospitalar Universitário de Lisboa Central, Lisboa, Portugal., Saraiva J; Medical Genetics Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal; Clinical Academic Center of Coimbra, Coimbra, Portugal; University Clinic of Pediatrics, Faculty of Medicine, Universidade de Coimbra, Coimbra, Portugal., Nishimura G; Intractable Disease Center, Saitama Medical University Moroyama Campus, Japan., Sousa SB; Medical Genetics Unit, Hospital Pediátrico, Centro Hospitalar e Universitário de Coimbra, Coimbra, Portugal; University Clinic of Genetics, Faculty of Medicine, Universidade de Coimbra, Coimbra, Portugal; Clinical Academic Center of Coimbra, Coimbra, Portugal. Electronic address: sbsousa@ulscoimbra.min-saude.pt.

المصدر: European journal of medical genetics [Eur J Med Genet] 2024 Apr; Vol. 68, pp. 104913. Date of Electronic Publication: 2024 Jan 28.

نوع المنشور: Case Reports

بيانات الدورية: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101247089 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-0849 (Electronic) Linking ISSN: 17697212 NLM ISO Abbreviation: Eur J Med Genet Subsets: MEDLINE

مواضيع طبية MeSH: Adenomatous Polyposis Coli*/genetics , Adenomatous Polyposis Coli*/diagnosis , Osteoma*/genetics, Male ; Humans ; Adolescent ; Adenomatous Polyposis Coli Protein/genetics ; Fibula/diagnostic imaging ; Fibula/pathology ; Genes, APC ; Germ-Line Mutation

المؤلفون: Vibert R; Department of Genetics, Institut Curie, Paris, France Roseline.VIBERT@aphp.fr.; PSL Research University, Paris, France., Le Gall J; Department of Genetics, Institut Curie, Paris, France.; Université de Paris, Paris, Île-de-France, France., Buecher B; Department of Genetics, Institut Curie, Paris, France.; PSL Research University, Paris, France., Mouret-Fourme E; Department of Genetics, Institut Curie, Paris, France.; PSL Research University, Paris, France., Bataillon G; PSL Research University, Paris, France.; Department of Pathology, Institut Curie, Paris, France., Becette V; PSL Research University, Paris, France.; Department of Pathology, Institut Curie, Paris, France., Trabelsi-Grati O; Department of Genetics, Institut Curie, Paris, France.; PSL Research University, Paris, France., Moncoutier V; Department of Genetics, Institut Curie, Paris, France.; PSL Research University, Paris, France., Dehainault C; Department of Genetics, Institut Curie, Paris, France.; PSL Research University, Paris, France., Carriere J; Department of Genetics, Institut Curie, Paris, France.; PSL Research University, Paris, France., Schwartz M; Department of Genetics, Institut Curie, Paris, France.; PSL Research University, Paris, France., Suybeng V; Department of Genetics, Institut Curie, Paris, France.; PSL Research University, Paris, France., Bieche I; Department of Genetics, Institut Curie, Paris, France.; Université de Paris, Paris, Île-de-France, France., Colas C; Department of Genetics, Institut Curie, Paris, France.; PSL Research University, Paris, France., Vincent-Salomon A; PSL Research University, Paris, France.; Department of Pathology, Institut Curie, Paris, France., Stoppa-Lyonnet D; Department of Genetics, Institut Curie, Paris, France.; Université de Paris, Paris, Île-de-France, France.; INSERM U830, Institut Curie, Paris, France., Golmard L; Department of Genetics, Institut Curie, Paris, France.; PSL Research University, Paris, France.

المصدر: Journal of medical genetics [J Med Genet] 2023 May; Vol. 60 (5), pp. 460-463. Date of Electronic Publication: 2022 Oct 21.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE

مواضيع طبية MeSH: Carcinoma, Ovarian Epithelial*/genetics , Genes, APC* , Ovarian Neoplasms*/genetics, Adult ; Female ; Humans ; Genetic Predisposition to Disease/genetics ; Germ Cells/pathology ; Germ-Line Mutation/genetics ; Premenopause ; beta Catenin/genetics

المؤلفون: Garside GB; Leibniz Institute on Aging, Fritz Lipmann Institute, 07745, Jena, Germany.; National Center for Tumor Diseases, 01307, Dresden, Germany., Sandoval M; Division of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, 98109, USA., Beronja S; Division of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, 98109, USA. beronja@fredhutch.org., Rudolph KL; Leibniz Institute on Aging, Fritz Lipmann Institute, 07745, Jena, Germany. lenhard.rudolph@leibniz-fli.de.

المصدر: BMC biology [BMC Biol] 2023 Jan 11; Vol. 21 (1), pp. 6. Date of Electronic Publication: 2023 Jan 11.

نوع المنشور: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 101190720 Publication Model: Electronic Cited Medium: Internet ISSN: 1741-7007 (Electronic) Linking ISSN: 17417007 NLM ISO Abbreviation: BMC Biol Subsets: MEDLINE

مواضيع طبية MeSH: Tumor Suppressor Protein p53*/metabolism , Genes, APC*, Mice ; Animals ; Mice, Transgenic ; Intestinal Mucosa/metabolism ; Stem Cells/metabolism

المؤلفون: Zeng M; Department of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China; School of Stomatology, Southern Medical University, Guangzhou 510515, China., Yao X; Department of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China; School of Stomatology, Southern Medical University, Guangzhou 510515, China., Pan Y; Stomatological Hospital, Southern Medical University, Guangzhou 510280, China., Gu H; Guangdong Provincial Key Laboratory of Gastroenterology, Department of Gastro Enterology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China., Xiong F; Department of Medical Genetics, School of Basic Medical Sciences, Southern Medical University, Guangzhou 510515, China; Guangdong Provincial Key Laboratory of Single Cell Technology and Application, Guangzhou, Guangdong, China; Department of Fetal Medicine and Prenatal Diagnosis, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong, China., Yin X; Department of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China. Electronic address: yinxm@smu.edu.cn., Wu B; Shenzhen Stomatological Hospital (Pingshan), Southern Medical University, Shenzhen 518118, China. Electronic address: bulingwu@smu.edu.cn., Chen T; Department of Stomatology, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China. Electronic address: chent@smu.edu.cn.

المصدر: Gene [Gene] 2024 Feb 20; Vol. 896, pp. 148051. Date of Electronic Publication: 2023 Dec 01.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Elsevier/North-Holland Country of Publication: Netherlands NLM ID: 7706761 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-0038 (Electronic) Linking ISSN: 03781119 NLM ISO Abbreviation: Gene Subsets: MEDLINE

مواضيع طبية MeSH: Adenomatous Polyposis Coli*/genetics , Adenomatous Polyposis Coli*/pathology , Gardner Syndrome*/genetics , Gardner Syndrome*/complications , Gardner Syndrome*/pathology , Odontoma*/complications , Odontoma*/genetics , Osteoma*/complications , Osteoma*/genetics, Humans ; Adenomatous Polyposis Coli Protein/genetics ; China ; Genes, APC ; Germ-Line Mutation ; Mutation

المؤلفون: Su L; Department of Thoracic Surgery, First Affiliated Hospital of Medical College, Shihezi University, Shihezi 832002, China., Huang H; Department of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin 300052, China., Gao M; Department of Thoracic Surgery, the Affiliated Hospital of Inner Mongolia Medical University, Hohhot 010030, China., Li Y; Tianjin Key Laboratory of 
Lung Cancer, Metastasis and Tumor Microenvironment, Tianjin Lung Cancer Institute, 
Tianjin Medical University General Hospital, Tianjin 300052, China., Shi R; Department of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin 300052, China., Chen C; Tianjin Key Laboratory of 
Lung Cancer, Metastasis and Tumor Microenvironment, Tianjin Lung Cancer Institute, 
Tianjin Medical University General Hospital, Tianjin 300052, China., Li X; Department of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin 300052, China., Zhu G; Department of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin 300052, China., Liu H; Tianjin Key Laboratory of 
Lung Cancer, Metastasis and Tumor Microenvironment, Tianjin Lung Cancer Institute, 
Tianjin Medical University General Hospital, Tianjin 300052, China., Chen J; Department of Thoracic Surgery, First Affiliated Hospital of Medical College, Shihezi University, Shihezi 832002, China.; Department of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin 300052, China.; Tianjin Key Laboratory of 
Lung Cancer, Metastasis and Tumor Microenvironment, Tianjin Lung Cancer Institute, 
Tianjin Medical University General Hospital, Tianjin 300052, China.

المصدر: Zhongguo fei ai za zhi = Chinese journal of lung cancer [Zhongguo Fei Ai Za Zhi] 2022 Sep 20; Vol. 25 (9), pp. 658-664.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Zhongguo fei ai za zhi bian ji wei yuan hui Country of Publication: China NLM ID: 101126433 Publication Model: Print Cited Medium: Internet ISSN: 1999-6187 (Electronic) Linking ISSN: 10093419 NLM ISO Abbreviation: Zhongguo Fei Ai Za Zhi Subsets: MEDLINE

مواضيع طبية MeSH: Cadherins*/genetics , Fanconi Anemia Complementation Group Proteins*/genetics , Genes, APC* , Genetic Predisposition to Disease* , Lung Neoplasms*/genetics, Antigens, CD/genetics ; Case-Control Studies ; China ; Gene Frequency ; Genotype ; Humans ; Polymorphism, Single Nucleotide

المؤلفون: Cai S; Cancer Institute, Key Laboratory of Cancer Prevention and Intervention, China National Ministry of Education.; Cancer Center, Zhejiang University., Yu Y; Cancer Center, Zhejiang University., Xie X; Cancer Center, Zhejiang University., Huang Y; Cancer Institute, Key Laboratory of Cancer Prevention and Intervention, China National Ministry of Education.; Cancer Center, Zhejiang University., Song Y; Cancer Institute, Key Laboratory of Cancer Prevention and Intervention, China National Ministry of Education., Zhan S; Cancer Institute, Key Laboratory of Cancer Prevention and Intervention, China National Ministry of Education.; Cancer Center, Zhejiang University., Zheng S; Cancer Institute, Key Laboratory of Cancer Prevention and Intervention, China National Ministry of Education.; Cancer Center, Zhejiang University.

المصدر: European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) [Eur J Cancer Prev] 2022 Sep 01; Vol. 31 (5), pp. 422-429. Date of Electronic Publication: 2022 Feb 21.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: England NLM ID: 9300837 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1473-5709 (Electronic) Linking ISSN: 09598278 NLM ISO Abbreviation: Eur J Cancer Prev Subsets: MEDLINE

مواضيع طبية MeSH: Adenomatous Polyposis Coli*/diagnosis , Adenomatous Polyposis Coli*/genetics , Genes, APC*, China ; Humans ; Hypertrophy/congenital ; Hypertrophy/diagnosis ; Hypertrophy/genetics ; Retinal Pigment Epithelium/pathology