المؤلفون: Liu D; Graduate School, Youjiang Medical University for Nationalities, Baise, Guangxi, China., Nong X; Center for Medical Laboratory Science, Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, Guangxi, China., Lai F; Graduate School, Youjiang Medical University for Nationalities, Baise, Guangxi, China., Nong C; Graduate School, Youjiang Medical University for Nationalities, Baise, Guangxi, China., Wang T; School of Medical Laboratory, Youjiang Medical University for Nationalities, Baise, Guangxi, China., Tang Y; School of Medical Laboratory, Youjiang Medical University for Nationalities, Baise, Guangxi, China.

المصدر: Hemoglobin [Hemoglobin] 2024 Mar; Vol. 48 (2), pp. 71-78. Date of Electronic Publication: 2024 Apr 18.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Informa Healthcare Country of Publication: England NLM ID: 7705865 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-432X (Electronic) Linking ISSN: 03630269 NLM ISO Abbreviation: Hemoglobin Subsets: MEDLINE

مواضيع طبية MeSH: Haplotypes*, Humans ; Female ; Pregnancy ; Thalassemia/genetics ; Thalassemia/diagnosis ; Databases, Genetic ; Prenatal Diagnosis/methods ; Noninvasive Prenatal Testing/methods ; Genotype ; China/epidemiology

المؤلفون: Chen M; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital, College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Provincial Key Laboratory of Prenatal Diagnosis and Birth Defect, Fuzhou, China., Lv A; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital, College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Provincial Key Laboratory of Prenatal Diagnosis and Birth Defect, Fuzhou, China., Zhang S; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital, College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Provincial Key Laboratory of Prenatal Diagnosis and Birth Defect, Fuzhou, China.; The School of Medical Technology and Engineering, Fujian Medical University, Fuzhou, China., Zheng J; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital, College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Provincial Key Laboratory of Prenatal Diagnosis and Birth Defect, Fuzhou, China.; The School of Medical Technology and Engineering, Fujian Medical University, Fuzhou, China., Zhang M; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital, College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Provincial Key Laboratory of Prenatal Diagnosis and Birth Defect, Fuzhou, China., Chen L; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital, College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Provincial Key Laboratory of Prenatal Diagnosis and Birth Defect, Fuzhou, China., He Q; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital, College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Provincial Key Laboratory of Prenatal Diagnosis and Birth Defect, Fuzhou, China., Zhuang J; Prenatal Diagnosis Center, Quanzhou Women's and Children's Hospital, Quanzhou, China., Lin N; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital, College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Provincial Key Laboratory of Prenatal Diagnosis and Birth Defect, Fuzhou, China., Xu L; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital, College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Provincial Key Laboratory of Prenatal Diagnosis and Birth Defect, Fuzhou, China., Huang H; Medical Genetic Diagnosis and Therapy Center, Fujian Maternity and Child Health Hospital, College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fujian Provincial Key Laboratory of Prenatal Diagnosis and Birth Defect, Fuzhou, China.; The School of Medical Technology and Engineering, Fujian Medical University, Fuzhou, China.

المصدر: Hemoglobin [Hemoglobin] 2024 Jan; Vol. 48 (1), pp. 34-38. Date of Electronic Publication: 2024 Jan 09.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Informa Healthcare Country of Publication: England NLM ID: 7705865 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-432X (Electronic) Linking ISSN: 03630269 NLM ISO Abbreviation: Hemoglobin Subsets: MEDLINE

مواضيع طبية MeSH: beta-Thalassemia*/diagnosis , beta-Thalassemia*/genetics , alpha-Thalassemia*/genetics, Pregnancy ; Female ; Humans ; Genotype ; Prenatal Diagnosis ; Mutation ; China

المؤلفون: Liu D; Graduate School, Youjiang Medical University for Nationalities, Baise, Guangxi, P.R. China., Nong C; Graduate School, Youjiang Medical University for Nationalities, Baise, Guangxi, P.R. China., Lai F; Graduate School, Youjiang Medical University for Nationalities, Baise, Guangxi, P.R. China., Tang Y; School of Medical Laboratory, Youjiang Medical University for Nationalities, Baise, Guangxi, P.R. China., Wang T; School of Medical Laboratory, Youjiang Medical University for Nationalities, Baise, Guangxi, P.R. China.

المصدر: Hemoglobin [Hemoglobin] 2023 Nov; Vol. 47 (2), pp. 80-84. Date of Electronic Publication: 2023 May 29.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: Informa Healthcare Country of Publication: England NLM ID: 7705865 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-432X (Electronic) Linking ISSN: 03630269 NLM ISO Abbreviation: Hemoglobin Subsets: MEDLINE

مواضيع طبية MeSH: Cell-Free Nucleic Acids* , beta-Thalassemia*/genetics, Child ; Pregnancy ; Humans ; Female ; DNA/genetics ; Prenatal Diagnosis/methods ; Fetus

المؤلفون: Tang HS; Prenatal Diagnosis Unit, Boai Hospital of Zhongshan, Zhongshan, Guangdong, People's Republic of China., Xiong Y; Prenatal Diagnosis Unit, Boai Hospital of Zhongshan, Zhongshan, Guangdong, People's Republic of China., Li DZ; Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center, Guangzhou, Guangdong, People's Republic of China.

المصدر: Hemoglobin [Hemoglobin] 2023 Nov; Vol. 47 (2), pp. 102-104. Date of Electronic Publication: 2023 May 29.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Informa Healthcare Country of Publication: England NLM ID: 7705865 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-432X (Electronic) Linking ISSN: 03630269 NLM ISO Abbreviation: Hemoglobin Subsets: MEDLINE

مواضيع طبية MeSH: alpha-Thalassemia*/complications , alpha-Thalassemia*/diagnosis , alpha-Thalassemia*/genetics , Hemoglobins, Abnormal*/genetics, Pregnancy ; Female ; Humans ; Hydrops Fetalis/diagnosis ; Hydrops Fetalis/etiology ; Hemoglobin H ; Fetal Hemoglobin ; Prenatal Diagnosis

المؤلفون: Singh P; Centre of Research for Development, Parul University, Vadodara, India., Shaikh S; Centre of Research for Development, Parul University, Vadodara, India., Parmar S; Centre of Research for Development, Parul University, Vadodara, India., Gupta R; Centre of Research for Development, Parul University, Vadodara, India.

المصدر: Hemoglobin [Hemoglobin] 2023 Sep; Vol. 47 (5), pp. 181-190. Date of Electronic Publication: 2023 Dec 07.

نوع المنشور: Journal Article; Review

بيانات الدورية: Publisher: Informa Healthcare Country of Publication: England NLM ID: 7705865 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-432X (Electronic) Linking ISSN: 03630269 NLM ISO Abbreviation: Hemoglobin Subsets: MEDLINE

مواضيع طبية MeSH: beta-Thalassemia*/diagnosis , beta-Thalassemia*/epidemiology , beta-Thalassemia*/genetics , Thalassemia*/diagnosis, Pregnancy ; Female ; Humans ; Prenatal Diagnosis ; Genetic Counseling ; India/epidemiology

المؤلفون: Aziz MA; Department of Biochemistry and Molecular Biology, Dhaka Shishu (Children) Hospital, Dhaka, Bangladesh., Khan WA; Department of Biochemistry and Molecular Biology, Dhaka Shishu (Children) Hospital, Dhaka, Bangladesh., Banu B; Department of Clinical Pathology, Dhaka Shishu (Children) Hospital, Dhaka, Bangladesh., Das SA; Department of Biochemistry and Molecular Biology, Dhaka Shishu (Children) Hospital, Dhaka, Bangladesh., Sadiya S; Department of Biochemistry and Molecular Biology, Dhaka Shishu (Children) Hospital, Dhaka, Bangladesh., Begum S; Department of Gynaecology and Obstetrics, Bangladesh Medical College and Hospital, Dhaka, Bangladesh.

المصدر: Hemoglobin [Hemoglobin] 2020 Nov; Vol. 44 (6), pp. 397-401. Date of Electronic Publication: 2020 Oct 22.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Informa Healthcare Country of Publication: England NLM ID: 7705865 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-432X (Electronic) Linking ISSN: 03630269 NLM ISO Abbreviation: Hemoglobin Subsets: MEDLINE

مواضيع طبية MeSH: Mutation* , Prenatal Diagnosis*/methods, alpha-Thalassemia/*diagnosis , alpha-Thalassemia/*genetics , beta-Thalassemia/*diagnosis , beta-Thalassemia/*genetics, Alleles ; Bangladesh/epidemiology ; Female ; Gene Frequency ; Genetic Loci ; Genotype ; Humans ; Male ; Pregnancy ; alpha-Thalassemia/epidemiology ; beta-Thalassemia/epidemiology

المؤلفون: Xu LL; Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong Province, People's Republic of China., Yang Y; Department of Obstetrics and Gynecology, Guangzhou Women and Children's Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong Province, People's Republic of China., Zhen L; Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong Province, People's Republic of China., Pan M; Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong Province, People's Republic of China., Han J; Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong Province, People's Republic of China., Zhou JY; Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong Province, People's Republic of China., Li DZ; Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center affiliated to Guangzhou Medical University, Guangzhou, Guangdong Province, People's Republic of China.

المصدر: Hemoglobin [Hemoglobin] 2020 Sep; Vol. 44 (5), pp. 325-328. Date of Electronic Publication: 2020 Aug 17.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Informa Healthcare Country of Publication: England NLM ID: 7705865 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-432X (Electronic) Linking ISSN: 03630269 NLM ISO Abbreviation: Hemoglobin Subsets: MEDLINE

مواضيع طبية MeSH: Prenatal Diagnosis*/methods, alpha-Thalassemia/*diagnosis , beta-Thalassemia/*diagnosis, Alleles ; China ; Female ; Gene Frequency ; Gestational Age ; Humans ; Mutation ; Pregnancy ; Retrospective Studies ; Tertiary Care Centers ; Time Factors ; alpha-Globins/genetics ; alpha-Thalassemia/genetics ; beta-Globins/genetics ; beta-Thalassemia/genetics

المؤلفون: Li J; Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, People's Republic of China., Jiang F; Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, People's Republic of China., Zhen L; Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, People's Republic of China., Tang XW; Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, People's Republic of China., Li DZ; Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, People's Republic of China.

المصدر: Hemoglobin [Hemoglobin] 2019 Jul - Sep; Vol. 43 (4-5), pp. 289-291. Date of Electronic Publication: 2019 Nov 05.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Informa Healthcare Country of Publication: England NLM ID: 7705865 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-432X (Electronic) Linking ISSN: 03630269 NLM ISO Abbreviation: Hemoglobin Subsets: MEDLINE

مواضيع طبية MeSH: Mutation* , Prenatal Diagnosis*, beta-Globins/*genetics , beta-Thalassemia/*genetics, Asian People ; Family ; Female ; Hemoglobin A2/analysis ; Heterozygote ; Humans ; Pregnancy

المؤلفون: Giambona A; Unit of Molecular Diagnostics of Rare Hematological Diseases, A.O.O.R. 'Villa Sofia Cervello', Palermo, Italy., Leto F; Unit of Molecular Diagnostics of Rare Hematological Diseases, A.O.O.R. 'Villa Sofia Cervello', Palermo, Italy., Cassarà F; Unit of Molecular Diagnostics of Rare Hematological Diseases, A.O.O.R. 'Villa Sofia Cervello', Palermo, Italy., Tartaglia V; Unit of Molecular Diagnostics of Rare Hematological Diseases, A.O.O.R. 'Villa Sofia Cervello', Palermo, Italy., Campisi R; Campisi Laboratories, Avola, Siracusa, Italy., Campisi C; Campisi Laboratories, Avola, Siracusa, Italy., Cigna V; Unit of Fetal Medicine and Prenatal Diagnosis, A.O.O.R. 'Villa Sofia Cervello', Palermo, Italy., Mugavero E; Unit of Fetal Medicine and Prenatal Diagnosis, A.O.O.R. 'Villa Sofia Cervello', Palermo, Italy., Cucinella G; Unit of Fetal Medicine and Prenatal Diagnosis, A.O.O.R. 'Villa Sofia Cervello', Palermo, Italy., Orlandi E; Unit of Fetal Medicine and Prenatal Diagnosis, A.O.O.R. 'Villa Sofia Cervello', Palermo, Italy., Picciotto F; Unit of Fetal Medicine and Prenatal Diagnosis, A.O.O.R. 'Villa Sofia Cervello', Palermo, Italy., Maggio A; Unit of Hematology for Rare Diseases of Blood and Blood-Forming Organs, Laboratory for Molecular Diagnosis and Rare Hematological Diseases, A.O.O.R. 'Villa Sofia Cervello', Palermo, Italy., Vinciguerra M; Unit of Molecular Diagnostics of Rare Hematological Diseases, A.O.O.R. 'Villa Sofia Cervello', Palermo, Italy.

المصدر: Hemoglobin [Hemoglobin] 2022 Nov; Vol. 46 (6), pp. 297-302. Date of Electronic Publication: 2023 Feb 21.

نوع المنشور: Case Reports; Journal Article

بيانات الدورية: Publisher: Informa Healthcare Country of Publication: England NLM ID: 7705865 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-432X (Electronic) Linking ISSN: 03630269 NLM ISO Abbreviation: Hemoglobin Subsets: MEDLINE

مواضيع طبية MeSH: beta-Thalassemia* , Thalassemia*, Female ; Humans ; Pregnancy ; Prenatal Diagnosis ; Early Diagnosis ; Fetus

المؤلفون: Chen X; Department of Laboratory Medicine, Guangxi Zhuang Autonomous Region People's Hospital, Nanning, People's Republic of China., Luo S; Department of Medical Genetics, Liuzhou Maternal and Child Health Hospital, Liuzhou, People's Republic of China., Huang J; Department of Medical Genetics, Liuzhou Maternal and Child Health Hospital, Liuzhou, People's Republic of China., Yuan D; Department of Medical Genetics, Liuzhou Maternal and Child Health Hospital, Liuzhou, People's Republic of China., Yan T; Department of Medical Genetics, Liuzhou Maternal and Child Health Hospital, Liuzhou, People's Republic of China., Cai R; Department of Medical Genetics, Liuzhou Maternal and Child Health Hospital, Liuzhou, People's Republic of China., Tang N; Department of Medical Genetics, Liuzhou Maternal and Child Health Hospital, Liuzhou, People's Republic of China.

المصدر: Hemoglobin [Hemoglobin] 2020 Jan; Vol. 44 (1), pp. 51-54. Date of Electronic Publication: 2020 Jan 14.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Informa Healthcare Country of Publication: England NLM ID: 7705865 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1532-432X (Electronic) Linking ISSN: 03630269 NLM ISO Abbreviation: Hemoglobin Subsets: MEDLINE

مواضيع طبية MeSH: Mutation* , Prenatal Diagnosis*, Hemoglobin A2/*genetics , Hemoglobin H/*genetics , alpha-Globins/*genetics , alpha-Thalassemia/*diagnosis , alpha-Thalassemia/*genetics, Adult ; Asian People ; Base Sequence ; Female ; Fetus ; Gene Expression ; Genetic Counseling ; Genotype ; Heterozygote ; Humans ; Male ; Pedigree ; Phenotype ; Sequence Analysis, DNA ; alpha-Thalassemia/ethnology ; alpha-Thalassemia/pathology