Familial 5p- syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1984.tb01091.x/fullpdf
Reference7 articles.
1. Cytologic observations in 35 individuals with a 5p- karyotype;Niebuhr;Hum. Genet.,1978a
2. The Cri-du-Chat Syndrome;Niebuhr;Hum. Genet.,1978b
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1. Three Offspring with Cri-du-Chat Syndrome from Phenotypically Normal Parents;Molecular Syndromology;2020
2. Multigenerational autosomal dominant inheritance of 5p chromosomal deletions;American Journal of Medical Genetics Part A;2015-11-24
3. Transmitted deletions of medial 5p and learning difficulties; Does the cadherin cluster only become penetrant when flanking genes are deleted?;American Journal of Medical Genetics Part A;2011-09-30
4. Familial Kleefstra syndrome due to maternal somatic mosaicism for interstitial 9q34.3 microdeletions;Clinical Genetics;2011-01-10
5. Partial 5p monosomy or trisomy in 11 patients from a family with a t(5;15)(p13.3;p12) translocation;Human Genetics;2008-09-07
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