المؤلفون: He Q; Hainan Provincial Key Laboratory for Human Reproductive Medicine and Genetic Research, Hainan Provincial Clinical Research Center for Thalassemia, the Key Laboratory of Tropical Translational Medicine of Ministry of Education, Department of Reproductive Medicine, the First Affiliated Hospital of Hainan Medical University, Hainan Medical University, Haikou, Hainan, 571101, China.; Haikou Key Laboratory for Preservation of Human Genetic Resource, the First Affiliated Hospital of Hainan Medical University, Haikou, Hainan, 571101, China., Zhang Y; Hainan Provincial Key Laboratory for Human Reproductive Medicine and Genetic Research, Hainan Provincial Clinical Research Center for Thalassemia, the Key Laboratory of Tropical Translational Medicine of Ministry of Education, Department of Reproductive Medicine, the First Affiliated Hospital of Hainan Medical University, Hainan Medical University, Haikou, Hainan, 571101, China.; Haikou Key Laboratory for Preservation of Human Genetic Resource, the First Affiliated Hospital of Hainan Medical University, Haikou, Hainan, 571101, China., Song M; Hainan Provincial Key Laboratory for Human Reproductive Medicine and Genetic Research, Hainan Provincial Clinical Research Center for Thalassemia, the Key Laboratory of Tropical Translational Medicine of Ministry of Education, Department of Reproductive Medicine, the First Affiliated Hospital of Hainan Medical University, Hainan Medical University, Haikou, Hainan, 571101, China.; Haikou Key Laboratory for Preservation of Human Genetic Resource, the First Affiliated Hospital of Hainan Medical University, Haikou, Hainan, 571101, China., Zhou Y; Hainan Provincial Key Laboratory for Human Reproductive Medicine and Genetic Research, Hainan Provincial Clinical Research Center for Thalassemia, the Key Laboratory of Tropical Translational Medicine of Ministry of Education, Department of Reproductive Medicine, the First Affiliated Hospital of Hainan Medical University, Hainan Medical University, Haikou, Hainan, 571101, China.; Haikou Key Laboratory for Preservation of Human Genetic Resource, the First Affiliated Hospital of Hainan Medical University, Haikou, Hainan, 571101, China., Lin D; Hainan Provincial Key Laboratory for Human Reproductive Medicine and Genetic Research, Hainan Provincial Clinical Research Center for Thalassemia, the Key Laboratory of Tropical Translational Medicine of Ministry of Education, Department of Reproductive Medicine, the First Affiliated Hospital of Hainan Medical University, Hainan Medical University, Haikou, Hainan, 571101, China.; Haikou Key Laboratory for Preservation of Human Genetic Resource, the First Affiliated Hospital of Hainan Medical University, Haikou, Hainan, 571101, China., Ma Y; Hainan Provincial Key Laboratory for Human Reproductive Medicine and Genetic Research, Hainan Provincial Clinical Research Center for Thalassemia, the Key Laboratory of Tropical Translational Medicine of Ministry of Education, Department of Reproductive Medicine, the First Affiliated Hospital of Hainan Medical University, Hainan Medical University, Haikou, Hainan, 571101, China. mayanlinma@163.com.; Haikou Key Laboratory for Preservation of Human Genetic Resource, the First Affiliated Hospital of Hainan Medical University, Haikou, Hainan, 571101, China. mayanlinma@163.com., Sun F; Hainan Provincial Key Laboratory for Human Reproductive Medicine and Genetic Research, Hainan Provincial Clinical Research Center for Thalassemia, the Key Laboratory of Tropical Translational Medicine of Ministry of Education, Department of Reproductive Medicine, the First Affiliated Hospital of Hainan Medical University, Hainan Medical University, Haikou, Hainan, 571101, China. 99609248@qq.com.; Haikou Key Laboratory for Preservation of Human Genetic Resource, the First Affiliated Hospital of Hainan Medical University, Haikou, Hainan, 571101, China. 99609248@qq.com.; Department of Obstetrics and Gynecology, Reproductive Medicine, Nanfang Hospital, Southern Medical University, Guangdong, 510515, China. 99609248@qq.com., Li Q; Hainan Provincial Key Laboratory for Human Reproductive Medicine and Genetic Research, Hainan Provincial Clinical Research Center for Thalassemia, the Key Laboratory of Tropical Translational Medicine of Ministry of Education, Department of Reproductive Medicine, the First Affiliated Hospital of Hainan Medical University, Hainan Medical University, Haikou, Hainan, 571101, China. 1315286326@qq.com.; Haikou Key Laboratory for Preservation of Human Genetic Resource, the First Affiliated Hospital of Hainan Medical University, Haikou, Hainan, 571101, China. 1315286326@qq.com.; Hainan Modern Women and Children's Hospital, Reproductive Medicine, Haikou, Hainan, 571101, China. 1315286326@qq.com.

المصدر: BMC urology [BMC Urol] 2024 Jun 12; Vol. 24 (1), pp. 123. Date of Electronic Publication: 2024 Jun 12.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: BioMed Central Country of Publication: England NLM ID: 100968571 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2490 (Electronic) Linking ISSN: 14712490 NLM ISO Abbreviation: BMC Urol Subsets: MEDLINE

مواضيع طبية MeSH: Chromosomes, Human, Y* , Infertility, Male*/genetics , Infertility, Male*/blood , Infertility, Male*/epidemiology , Chromosome Deletion* , Sex Chromosome Aberrations* , Sex Chromosome Disorders of Sex Development*/blood , Sex Chromosome Disorders of Sex Development*/genetics , Sex Chromosome Disorders of Sex Development*/epidemiology , Reproductive Techniques, Assisted*, Humans ; Male ; China/epidemiology ; Adult ; Luteinizing Hormone/blood ; Follicle Stimulating Hormone/blood ; Azoospermia/genetics ; Azoospermia/blood ; Prolactin/blood ; Oligospermia/genetics ; Oligospermia/blood ; Testosterone/blood ; Estradiol/blood ; Semen Analysis

SCR Disease Name: Male sterility due to Y-chromosome deletions

المؤلفون: Liu S; Department of Reproductive Andrology/Human Sperm Bank, MoE Key Laboratory of Birth Defects and Related Diseases of Women and Children, West China Second University Hospital, Sichuan University, Chengdu, Sichuan 610041, China. lfpsnake@scu.edu.cn., Xian Y, Li F

المصدر: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics [Zhonghua Yi Xue Yi Chuan Xue Za Zhi] 2024 May 10; Vol. 41 (5), pp. 513-518.

نوع المنشور: English Abstract; Journal Article

بيانات الدورية: Publisher: Sichuan University Country of Publication: China NLM ID: 9425197 Publication Model: Print Cited Medium: Print ISSN: 1003-9406 (Print) Linking ISSN: 10039406 NLM ISO Abbreviation: Zhonghua Yi Xue Yi Chuan Xue Za Zhi Subsets: MEDLINE

مواضيع طبية MeSH: Chromosomes, Human, Y*/genetics , Chromosome Deletion* , Infertility, Male*/genetics , Sex Chromosome Aberrations* , Oligospermia*/genetics , Karyotyping* , Azoospermia*/genetics , Sex Chromosome Disorders of Sex Development*/genetics, Humans ; Male ; China ; Adult ; Retrospective Studies ; Abnormal Karyotype ; Young Adult

SCR Disease Name: Male sterility due to Y-chromosome deletions

المؤلفون: Cieslak J; Department of Genetics and Animal Breeding, Poznan University of Life Sciences, Wolynska 33, 60-637, Poznan, Poland. jakub.cieslak@up.poznan.pl., Mackowski M; Department of Genetics and Animal Breeding, Poznan University of Life Sciences, Wolynska 33, 60-637, Poznan, Poland., Skrzetuska W; Department of Genetics and Animal Breeding, Poznan University of Life Sciences, Wolynska 33, 60-637, Poznan, Poland., Fidos-Tama E; Vet4horse, Chabrowa 95 BC, 55-200, Wysoka, Poland., Siwinska N; Department of Internal Medicine and Clinic of Diseases of Horses, Dogs and Cats, Wroclaw University of Environmental and Life Sciences, Wroclaw, Poland., Szczerbal I; Department of Genetics and Animal Breeding, Poznan University of Life Sciences, Wolynska 33, 60-637, Poznan, Poland.

المصدر: Journal of applied genetics [J Appl Genet] 2024 May; Vol. 65 (2), pp. 395-398. Date of Electronic Publication: 2024 Feb 17.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Springer Country of Publication: England NLM ID: 9514582 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2190-3883 (Electronic) Linking ISSN: 12341983 NLM ISO Abbreviation: J Appl Genet Subsets: MEDLINE

مواضيع طبية MeSH: Sex Chromosome Aberrations*/veterinary , Sex Chromosome Disorders of Sex Development* , Trisomy*/genetics, Animals ; Female ; Chromosomes, Human, X ; Cytogenetic Analysis ; Horses/genetics

SCR Disease Name: Triple X syndrome

المؤلفون: Ng R; Department of Obstetrics and Gynaecology, University of British Columbia, Vancouver, BC, Canada., Stanar P; Department of Obstetrics and Gynaecology, University of British Columbia, Vancouver, BC, Canada., Louie K; Department of Obstetrics and Gynaecology, University of British Columbia, Vancouver, BC, Canada., Chow V; Department of Obstetrics and Gynaecology, University of British Columbia, Vancouver, BC, Canada., Ma S; Department of Obstetrics and Gynaecology, University of British Columbia, Vancouver, BC, Canada. Electronic address: msai914@gmail.com.

المصدر: Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC [J Obstet Gynaecol Can] 2024 Apr; Vol. 46 (4), pp. 102342. Date of Electronic Publication: 2024 Jan 02.

نوع المنشور: Journal Article; Comparative Study

بيانات الدورية: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101126664 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1701-2163 (Print) Linking ISSN: 17012163 NLM ISO Abbreviation: J Obstet Gynaecol Can Subsets: MEDLINE

مواضيع طبية MeSH: Chromosomes, Human, Y*/genetics , Chromosome Deletion* , Fetal Blood*/chemistry , Sex Chromosome Disorders of Sex Development*/genetics , Sex Chromosome Disorders of Sex Development*/blood , Sex Chromosome Aberrations* , Sperm Injections, Intracytoplasmic* , Infertility, Male*/genetics, Humans ; Male ; Infant, Newborn ; Fertilization in Vitro ; Adult ; Female

SCR Disease Name: Male sterility due to Y-chromosome deletions

المؤلفون: Tangtanatakul P; Department of Transfusion Medicine and Clinical Microbiology, Faculty of Allied Health Sciences, Chulalongkorn University, Bangkok, Thailand.; Centre of Excellent in Immunology and Immune-Mediated Diseases, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand., Lei Y; Department of Paediatrics and Adolescent Medicine, Hong Kong University, Hong Kong, People's Republic of China., Jaiwan K; Master of Sciences Program in Molecular Science of Medical Microbiology and Immunology, Faculty of Allied Health Sciences, Chulalongkorn University, Bangkok, Thailand., Yang W; Department of Paediatrics and Adolescent Medicine, Hong Kong University, Hong Kong, People's Republic of China., Boonbangyang M; National Biobank of Thailand (NBT), National Science and Technology Development Agency, Khlong Luang, Pathum Thani, Thailand., Kunhapan P; Department of Medical Sciences, Ministry of Public Health, Nonthaburi, Thailand., Sodsai P; Centre of Excellent in Immunology and Immune-Mediated Diseases, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.; Division of Immunology, Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand., Mahasirimongkol S; Department of Medical Sciences, Ministry of Public Health, Nonthaburi, Thailand., Pisitkun P; Division of Allergy, Immunology, and Rheumatology, Department of Medicine, Mahidol University Faculty of Medicine Ramathibodi Hospital, Bangkok, Thailand., Yang Y; Department of Nephrology, Fourth Affiliated Hospital, International Institutes of Medicine, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China., Eu-Ahsunthornwattana J; Department of Community Medicine, Mahidol University Faculty of Medicine Ramathibodi Hospital, Bangkok, Thailand., Aekplakorn W; Department of Community Medicine, Mahidol University Faculty of Medicine Ramathibodi Hospital, Bangkok, Thailand., Jinawath N; Program in Translational Medicine, Mahidol University Faculty of Medicine Ramathibodi Hospital, Bangkok, Thailand.; Integrative Computational BioScience (ICBS) Center, Mahidol University, Nakornpathom, Thailand., Neelapaichit N; Ramathibodi School of Nursing, Mahidol University Faculty of Medicine Ramathibodi Hospital, Bangkok, Thailand., Hirankarn N; Centre of Excellent in Immunology and Immune-Mediated Diseases, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.; Division of Immunology, Department of Microbiology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand., Wang YF; Warshel Institute for Computational Biology, The Chinese University of Hong Kong, Shenzhen, Guangdong, People's Republic of China yfwang@cuhk.edu.cn.; School of Medicine, The Chinese University of Hong Kong, Shenzhen, Guangdong, People's Republic of China.

المصدر: Lupus science & medicine [Lupus Sci Med] 2024 Mar 08; Vol. 11 (1). Date of Electronic Publication: 2024 Mar 08.

نوع المنشور: Meta-Analysis; Journal Article

بيانات الدورية: Publisher: BMJ Country of Publication: England NLM ID: 101633705 Publication Model: Electronic Cited Medium: Print ISSN: 2053-8790 (Print) Linking ISSN: 20538790 NLM ISO Abbreviation: Lupus Sci Med Subsets: MEDLINE

مواضيع طبية MeSH: Lupus Erythematosus, Systemic*/epidemiology , Lupus Erythematosus, Systemic*/genetics , Trisomy* , Sex Chromosome Disorders of Sex Development*, Humans ; Male ; Female ; Genetic Predisposition to Disease ; Thailand/epidemiology ; Sex Chromosome Aberrations ; Chromosomes, Human, X/genetics ; China ; Membrane Proteins

SCR Disease Name: Triple X syndrome

المؤلفون: Davis SM; Department of Pediatrics, University of Colorado School of Medicine, Aurora.; eXtraOrdinarY Kids Clinic, Children's Hospital Colorado, Aurora., Teerlink C; VA Informatics and Computing Infrastructure, VA Salt Lake City Healthcare System, Salt Lake City, Utah.; Department of Internal Medicine, University of Utah Health, Salt Lake City., Lynch JA; VA Informatics and Computing Infrastructure, VA Salt Lake City Healthcare System, Salt Lake City, Utah.; Department of Internal Medicine, University of Utah Health, Salt Lake City.; College of Nursing and Health Sciences, University of Massachusetts, Lowell., Gorman BR; VA Boston Healthcare System, Boston, Massachusetts., Pagadala M; Medical Scientist Training Program, University of California San Diego, La Jolla.; Biomedical Science Program, University of California San Diego, La Jolla., Liu A; University of Helsinki Institute for Molecular Medicine, Helsinki, Finland., Panizzon MS; Center for Behavioral Genetics of Aging, School of Medicine, University of California San Diego, La Jolla., Merritt VC; Department of Psychiatry, University of California San Diego, La Jolla.; Center of Excellence for Stress and Mental Health, VA San Diego Healthcare System, San Diego, California., Genovese G; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Boston, Massachusetts.; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, Massachusetts.; Department of Genetics, Harvard Medical School, Boston, Massachusetts., Ross JL; Nemours Children's Hospital Delaware, Wilmington.; Department of Pediatrics, School of Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania., Hauger RL; Center for Behavioral Genetics of Aging, School of Medicine, University of California San Diego, La Jolla.; Center of Excellence for Stress and Mental Health, VA San Diego Healthcare System, San Diego, California.

المصدر: JAMA network open [JAMA Netw Open] 2024 Mar 04; Vol. 7 (3), pp. e244113. Date of Electronic Publication: 2024 Mar 04.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: American Medical Association Country of Publication: United States NLM ID: 101729235 Publication Model: Electronic Cited Medium: Internet ISSN: 2574-3805 (Electronic) Linking ISSN: 25743805 NLM ISO Abbreviation: JAMA Netw Open Subsets: MEDLINE

مواضيع طبية MeSH: Veterans* , XYY Karyotype* , Sex Chromosome Disorders*, Male ; Humans ; Female ; Prevalence ; Case-Control Studies ; Cross-Sectional Studies ; Quality of Life ; Sex Chromosome Aberrations ; Aneuploidy ; Morbidity ; Sex Chromosomes

SCR Disease Name: 47, XYY syndrome

المؤلفون: Krausz C; Department of Experimental and Clinical Biomedical Sciences 'Mario Serio', University of Florence, University Hospital Careggi, Florence, Italy., Navarro-Costa P; EvoReproMed Lab, Environmental Health Institute (ISAMB), Associate Laboratory TERRA, Faculty of Medicine, University of Lisbon, Lisbon, Portugal.; Gulbenkian Science Institute, Oeiras, Portugal., Wilke M; Department of Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands., Tüttelmann F; Institute of Reproductive Genetics, University of Münster, Münster, Germany.

المصدر: Andrology [Andrology] 2024 Mar; Vol. 12 (3), pp. 487-504. Date of Electronic Publication: 2023 Sep 06.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 101585129 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2047-2927 (Electronic) Linking ISSN: 20472919 NLM ISO Abbreviation: Andrology Subsets: MEDLINE

مواضيع طبية MeSH: Andrology* , Infertility, Male*/diagnosis , Infertility, Male*/genetics , Infertility, Male*/pathology , Azoospermia*/diagnosis , Azoospermia*/genetics , Azoospermia*/pathology , Oligospermia*/diagnosis , Oligospermia*/genetics , Sertoli Cell-Only Syndrome*/genetics , Sex Chromosome Aberrations* , Sex Chromosome Disorders of Sex Development*, Humans ; Male ; Semen ; Chromosome Deletion ; Chromosomes, Human, Y/genetics ; Multiplex Polymerase Chain Reaction

SCR Disease Name: Male sterility due to Y-chromosome deletions

المؤلفون: Sone I; Department of Plastic and Reconstructive Surgery, School of Medicine, Iwate Medical University, Morioka, Japan., Honda T; Department of Plastic and Reconstructive Surgery, School of Medicine, Iwate Medical University, Morioka, Japan., Sakuraba M; Department of Plastic and Reconstructive Surgery, School of Medicine, Iwate Medical University, Morioka, Japan., Satoh K; Division of Orthodontics, Department of Developmental Oral Health Science, School of Dentistry, Iwate Medical University, Morioka, Japan., Kuwajima Y; Division of Orthodontics, Department of Developmental Oral Health Science, School of Dentistry, Iwate Medical University, Morioka, Japan., Baba S; Department of Dermatology, School of Medicine, Iwate Medical University, Morioka, Japan., Wada Y; Department of Pediatrics, School of Medicine, Iwate Medical University, Morioka, Japan.

المصدر: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association [Cleft Palate Craniofac J] 2024 Mar; Vol. 61 (3), pp. 534-538. Date of Electronic Publication: 2022 Nov 28.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: SAGE Publications in Association with American Cleft Palate-Craniofacial Association Country of Publication: United States NLM ID: 9102566 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1545-1569 (Electronic) Linking ISSN: 10556656 NLM ISO Abbreviation: Cleft Palate Craniofac J Subsets: MEDLINE

مواضيع طبية MeSH: Focal Dermal Hypoplasia*/genetics , Focal Dermal Hypoplasia*/diagnosis , Cleft Palate* , Syndactyly* , Trisomy* , Sex Chromosome Disorders of Sex Development*, Humans ; Infant, Newborn ; Male ; Female ; Sex Chromosome Aberrations ; Syndrome ; Chromosomes, Human, X

SCR Disease Name: Triple X syndrome

المؤلفون: Graziani A; Department of Medicine, University of Padova, Padova, Italy., Merico M; Department of Systems Medicine, Unit of Andrology and Reproductive Medicine, University Hospital of Padova, Padova, Italy., Grande G; Department of Systems Medicine, Unit of Andrology and Reproductive Medicine, University Hospital of Padova, Padova, Italy., Di Mambro A; Department of Systems Medicine, Unit of Andrology and Reproductive Medicine, University Hospital of Padova, Padova, Italy., Vinanzi C; Department of Systems Medicine, Unit of Andrology and Reproductive Medicine, University Hospital of Padova, Padova, Italy., Rocca MS; Department of Systems Medicine, Unit of Andrology and Reproductive Medicine, University Hospital of Padova, Padova, Italy., Selice R; Department of Systems Medicine, Unit of Andrology and Reproductive Medicine, University Hospital of Padova, Padova, Italy., Ferlin A; Department of Medicine, University of Padova, Padova, Italy.; Department of Systems Medicine, Unit of Andrology and Reproductive Medicine, University Hospital of Padova, Padova, Italy.

المصدر: Human reproduction (Oxford, England) [Hum Reprod] 2024 Mar 01; Vol. 39 (3), pp. 504-508.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Oxford University Press Country of Publication: England NLM ID: 8701199 Publication Model: Print Cited Medium: Internet ISSN: 1460-2350 (Electronic) Linking ISSN: 02681161 NLM ISO Abbreviation: Hum Reprod Subsets: MEDLINE

مواضيع طبية MeSH: Infertility, Male*/genetics , Oligospermia*/genetics , Chromosome Deletion* , Sex Chromosome Aberrations* , Sex Chromosome Disorders of Sex Development*, Humans ; Male ; Polymorphism, Single Nucleotide ; Semen ; Follicle Stimulating Hormone, beta Subunit/genetics ; Chromosomes, Human, Y/genetics

SCR Disease Name: Male sterility due to Y-chromosome deletions

المؤلفون: Tang X; Department of Prenatal Diagnosis, Lianyungang Maternal and Child Health Hospital, Lianyungang, Jiangsu 222000, People's Republic of China., Du Y; Department of Prenatal Diagnosis, Lianyungang Maternal and Child Health Hospital, Lianyungang, Jiangsu 222000, People's Republic of China., Chen M; Department of Prenatal Diagnosis, Lianyungang Maternal and Child Health Hospital, Lianyungang, Jiangsu 222000, People's Republic of China., Zhang Y; Department of Prenatal Diagnosis, Lianyungang Maternal and Child Health Hospital, Lianyungang, Jiangsu 222000, People's Republic of China., Wang Z; Department of Prenatal Diagnosis, Lianyungang Maternal and Child Health Hospital, Lianyungang, Jiangsu 222000, People's Republic of China., Zhang F; Department of Prenatal Diagnosis, Lianyungang Maternal and Child Health Hospital, Lianyungang, Jiangsu 222000, People's Republic of China., Tan J; Department of Prenatal Diagnosis, Lianyungang Maternal and Child Health Hospital, Lianyungang, Jiangsu 222000, People's Republic of China., Yin T; Department of Prenatal Diagnosis, Lianyungang Maternal and Child Health Hospital, Lianyungang, Jiangsu 222000, People's Republic of China., Wang L; Department of Prenatal Diagnosis, Lianyungang Maternal and Child Health Hospital, Lianyungang, Jiangsu 222000, People's Republic of China. Electronic address: wangleileiok@hotmail.com.

المصدر: Clinica chimica acta; international journal of clinical chemistry [Clin Chim Acta] 2024 Feb 01; Vol. 554, pp. 117770. Date of Electronic Publication: 2024 Jan 08.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 1302422 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1873-3492 (Electronic) Linking ISSN: 00098981 NLM ISO Abbreviation: Clin Chim Acta Subsets: MEDLINE

مواضيع طبية MeSH: Trisomy*/diagnosis , Trisomy*/genetics , Turner Syndrome*/diagnosis , Turner Syndrome*/genetics , Sex Chromosome Disorders of Sex Development*, Female ; Humans ; Pregnancy ; Male ; Mosaicism ; DNA Copy Number Variations ; Retrospective Studies ; Sex Chromosome Aberrations ; Prenatal Diagnosis/methods ; Chromosomes, Human, X/genetics ; Aneuploidy

SCR Disease Name: Triple X syndrome