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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Bibliografiske detaljer
Udgivet i:Case Rep Genet
Main Authors: Puvabanditsin, Surasak, Sadiq, Mehrin, Jacob, Marianne, Jalil, Maaz, Cabrera, Kenya, Choudry, Omer, Mehta, Rajeev
Format: Artigo
Sprog:Inglês
Udgivet: Hindawi 2018
Fag:
Case Report
Online adgang: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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