المؤلفون: Ramanujam, Lakshmi, Liao, Wu-Xiang, Roy, Ashim C., Ng, Soon Chye, Ratnam, Shan S.

المصدر: Human Heredity, 1998 Jan 01. 48(4), 232-234.

URL الوصول: https://www.jstor.org/stable/48506193

المؤلفون: Shan S. Ratnam, Ashim C. Roy, Lakshmi Ramanujam, Soon-Chye Ng, W.-X. Liao

المصدر: Human Heredity. 48:232-234

مصطلحات موضوعية: Male, medicine.drug_class, Population genetics, Biology, medicine.disease_cause, Polymerase Chain Reaction, Exon, Asian People, Gene Frequency, Polymorphism (computer science), Genetics, medicine, Humans, Allele frequency, Alleles, Asia, Southeastern, Genetics (clinical), Mutation, Female infertility, Sequence Analysis, DNA, Luteinizing Hormone, medicine.disease, Genetics, Population, Female, Gonadotropin, Luteinizing hormone, Polymorphism, Restriction Fragment Length

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f887d8dab57ce6c7306bbbfeb5a0efd
https://doi.org/10.1159/000022807

المؤلفون: Nilmani Saha, Ashim C. Roy, John S. H. Tay, Shan S. Ratnam

المصدر: Human heredity. 41(4)

مصطلحات موضوعية: Genetics, Singapore, Polymorphism, Genetic, Paraoxon, Aryldialkylphosphatase, Metabolite, Biology, Hydrogen-Ion Concentration, Hardy–Weinberg principle, PON1, Phosphoric Monoester Hydrolases, Arylesterase, chemistry.chemical_compound, Parathion, chemistry, Polymorphism (computer science), medicine, Humans, Allele, Genetics (clinical), medicine.drug

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8bd1733ff09148aa6ef9acc7d14f7697
https://pubmed.ncbi.nlm.nih.gov/1664414

المؤلفون: Chen S; Institute of Maternal and Child Medicine Research, Affiliated Shenzhen Maternity and Child Healthcare Hospital, Southern Medical University, Shenzhen, China.; Laboratory of Molecular Medicine, Shenzhen Health Development Research Center, Shenzhen, China., Gao J; Institute of Maternal and Child Medicine Research, Affiliated Shenzhen Maternity and Child Healthcare Hospital, Southern Medical University, Shenzhen, China., Wu Q; Institute of Maternal and Child Medicine Research, Affiliated Shenzhen Maternity and Child Healthcare Hospital, Southern Medical University, Shenzhen, China., Li X; Laboratory of Molecular Medicine, Shenzhen Health Development Research Center, Shenzhen, China., Lin S; Laboratory of Molecular Medicine, Shenzhen Health Development Research Center, Shenzhen, China., Su J; Institute of Maternal and Child Medicine Research, Affiliated Shenzhen Maternity and Child Healthcare Hospital, Southern Medical University, Shenzhen, China., Zheng K; Institute of Maternal and Child Medicine Research, Affiliated Shenzhen Maternity and Child Healthcare Hospital, Southern Medical University, Shenzhen, China., Guo Z; Departments of Laboratory Medicine, Shenzhen Luohu Maternity and Child Healthcare Hospital, Shenzhen, China., Yao J; Institute of Maternal and Child Medicine Research, Affiliated Shenzhen Maternity and Child Healthcare Hospital, Southern Medical University, Shenzhen, China., Duan S; Institute of Maternal and Child Medicine Research, Affiliated Shenzhen Maternity and Child Healthcare Hospital, Southern Medical University, Shenzhen, China.

المصدر: Human heredity [Hum Hered] 2023; Vol. 88 (1), pp. 1-7. Date of Electronic Publication: 2022 Oct 31.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Karger Country of Publication: Switzerland NLM ID: 0200525 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1423-0062 (Electronic) Linking ISSN: 00015652 NLM ISO Abbreviation: Hum Hered Subsets: MEDLINE

مواضيع طبية MeSH: Glucosephosphate Dehydrogenase*/genetics , Glucosephosphate Dehydrogenase Deficiency*/diagnosis , Glucosephosphate Dehydrogenase Deficiency*/genetics , Glucosephosphate Dehydrogenase Deficiency*/epidemiology, Female ; Humans ; Missed Diagnosis ; Mutation ; Polymerase Chain Reaction/methods ; Retrospective Studies

المؤلفون: Gao J; Laboratory of Molecular Medicine, Shenzhen Health Development Research Center, Shenzhen, China, 303661087@qq.com., Lin S; Laboratory of Molecular Medicine, Shenzhen Health Development Research Center, Shenzhen, China., Chen S; Laboratory of Molecular Medicine, Shenzhen Health Development Research Center, Shenzhen, China., Wu Q; Laboratory of Molecular Medicine, Shenzhen Health Development Research Center, Shenzhen, China., Zheng K; Laboratory of Molecular Medicine, Shenzhen Health Development Research Center, Shenzhen, China., Su J; Laboratory of Molecular Medicine, Shenzhen Health Development Research Center, Shenzhen, China., Guo Z; Shenzhen Luohu Maternity and Child Healthcare Hospital, Shenzhen, China., Duan S; Laboratory of Molecular Medicine, Shenzhen Health Development Research Center, Shenzhen, China.

المصدر: Human heredity [Hum Hered] 2020; Vol. 85 (3-6), pp. 110-116. Date of Electronic Publication: 2021 Jun 16.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Karger Country of Publication: Switzerland NLM ID: 0200525 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1423-0062 (Electronic) Linking ISSN: 00015652 NLM ISO Abbreviation: Hum Hered Subsets: PubMed not MEDLINE; MEDLINE