11p15.4 Microdeletion Associates with Hemihypertrophy

We report a preterm female infant with intrauterine growth retardation, dysmorphic facies, missing rib, small hands and feet, and hemihypertrophy. The results of whole genome SNP microarray analysis showed approximately 77 Kb interstitial deletion of the short arm of chromosome 11 (11p15.4). We repo...

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Detalhes bibliográficos
Publicado no:Case Rep Genet
Main Authors: Puvabanditsin, Surasak, Sadiq, Mehrin, Jacob, Marianne, Jalil, Maaz, Cabrera, Kenya, Choudry, Omer, Mehta, Rajeev
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi 2018
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6232786/
https://ncbi.nlm.nih.gov/pubmed/30510815
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2018/2746347
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