Molecular refinement of the 1p36 deletion syndrome reveals size diversity and a preponderance of maternally derived deletions
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/8/2/313/1572407/8-2-313.pdf
Cited by 87 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. Implication of Genetic Testing and Pregnancy Outcome in a Woman with Unbalanced Translocation t(1;6);American Journal of Case Reports;2022-01-17
2. Chromosome 1p36 Deletion Syndrome: Four Patients with Variable Presentations;Journal of Pediatric Genetics;2021-07-28
3. SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females;The American Journal of Human Genetics;2021-03
4. DELETION 1p36 SYNDROME;Cassidy and Allanson's Management of Genetic Syndromes;2020-10-30
5. Deep Phenotyping in 1p36 Deletion Syndrome;Annals of Child Neurology;2020-10-01
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