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Phenotypic Variations in Wolf-Hirschhorn Syndrome

Wolf-Hirschhorn syndrome (WHS) is a rare chromosomal disorder caused by terminal deletion of the short arm of chromosome 4. The clinical picture includes growth retardation, severe mental retardation, characteristic “Greek helmet” like face, seizures and midline defects in the brain, heart, palate a...

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Detalhes bibliográficos
Publicado no:Balkan J Med Genet
Main Authors: Sukarova-Angelovska, E, Kocova, M, Sabolich, V, Palcevska, S, Angelkova, N
Formato: Artigo
Idioma:Inglês
Publicado em: Macedonian Science of Sciences and Arts 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4347473/
https://ncbi.nlm.nih.gov/pubmed/25741211
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2478/bjmg-2014-0021
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