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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 7 (of 7 Records)

Query Trace: Birth Weight and AR[original query]
Effects of the Trp64Arg polymorphism in the beta3-adrenergic receptor gene on insulin sensitivity in small for gestational age neonates.
The Journal of clinical endocrinology and metabolism 2004 Oct 89 (10): 4981-5.
Wang Xinli, Cui Yunpu, Tong Xiaomei, Ye Hongmao, Li So
Flutamide metformin for post-menarcheal girls with preclinical ovarian androgen excess: evidence for differential response by androgen receptor genotype.
European journal of endocrinology / European Federation of Endocrine Societies 2007 Nov 157 (5): 661-8.
Ong Ken K, de Zegher Francis, López-Bermejo Abel, Dunger David B, Ibáñez Lourd
[Influence of angiotensin converting enzyme gene insertion/deletion polymorphism and beta3-adrenergic receptor gene Trp64Arg polymorphism on fetal growth and neonatal insulin sensitivity].
Zhonghua er ke za zhi. Chinese journal of pediatrics 2008 Jun 46 (6): 421-7.
Cui Yun-pu, Han Tong-yan, Wang Xin-li, Ye Hong-m
Low frequency of androgen receptor gene mutations in 46 XY DSD, and fetal growth restriction.
Archives of disease in childhood 2014 Apr 99 (4): 358-61.
Lek Ngee, Miles Harriet, Bunch Trevor, Pilfold-Wilkie Vickie, Tadokoro-Cuccaro Rieko, Davies John, Ong Ken K, Hughes Ieuan
Microsatellite polymorphisms associated with human behavioural and psychological phenotypes including a gene-environment interaction.
BMC medical genetics 2017 Feb 18 (1): 12.
Bagshaw Andrew T M, Horwood L John, Fergusson David M, Gemmell Neil J, Kennedy Martin
Association between perinatal factors, genetic susceptibility to obesity and age at adiposity rebound in children of the EDEN mother-child cohort.
International journal of obesity (2005) 2021 May .
Cissé Aminata Hallimat, Lioret Sandrine, de Lauzon-Guillain Blandine, Forhan Anne, Ong Ken K, Charles Marie Aline, Heude Barba
Mutations in AR or SRD5A2 Genes: Clinical Findings, Endocrine Pitfalls, and Genetic Features of Children with 46,XY DSD.
Journal of clinical research in pediatric endocrinology 2022 2 14 (2): 153-171.
Akcan Ne?e, Uyguner Oya, Ba? Firdevs, Altuno?lu Umut, Toksoy Güven, Karaman Birsen, Avc? ?ahin, Yava? Abal? Zehra, Poyrazo?lu ?ükran, Aghayev Agharza, Karaman Volkan, Bundak Rüveyde, Ba?aran Seher, Darendeliler Fey
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