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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Bibliografski detalji
Izdano u:Case Rep Genet
Glavni autori: Puvabanditsin, Surasak, Sadiq, Mehrin, Jacob, Marianne, Jalil, Maaz, Cabrera, Kenya, Choudry, Omer, Mehta, Rajeev
Format: Artigo
Jezik:Inglês
Izdano: Hindawi 2018
Teme:
Case Report
Online pristup: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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