Birth seasonality in Prader-Willi syndrome resulting from chromosome 15 microdeletion
Author:
Affiliation:
1. Department of Pediatrics; Dokkyo Medical University Koshigaya Hospital; Koshigaya; Japan
2. Department of Molecular Endocrinology; National Research Institute for Child Health and Development; Tokyo; Japan
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.35893/fullpdf
Reference14 articles.
1. Homologous recombination as a mechanism for genome rearrangements: Environmental and genetic effects;Bishop;Hum Mol Genet,2000
2. Birth seasonality in Prader-Willi syndrome;Butler;Lancet,1985
3. Prader-Willi syndrome;Cassidy;Eur J Hum Genet,2009
4. A deletion of the HBII-85 class of small nucleolar RNAs (snoRNAs) is associated with hyperphagia, obesity and hypogonadism;de Smith;Hum Mol Genet,2009
5. Clinical evidence of intrauterine disturbance in Prader-Willi syndrome, a genetically imprinted neurodevelopmental disorder;Dudley;Early Hum Dev,2007
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Established and Novel Mechanisms Leading to de novo Genomic Rearrangements in the Human Germline;Cytogenetic and Genome Research;2020
2. Birth seasonality studies in a large Prader-Willi syndrome cohort;American Journal of Medical Genetics Part A;2019-06-21
3. Frequency of Common Copy-Number Variations at 15q11.2q13 in Sperm of Healthy Men;Cytogenetic and Genome Research;2019
4. Birth seasonality in Korean Prader-Willi syndrome with chromosome 15 microdeletion;Annals of Pediatric Endocrinology & Metabolism;2015
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