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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Detalles Bibliográficos
Autores principales: Sukarova-Angelovska, E, Kocova, M, Sabolich, V, Palcevska, S, Angelkova, N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Macedonian Science of Sciences and Arts 2014
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4347473/
https://www.ncbi.nlm.nih.gov/pubmed/25741211
http://dx.doi.org/10.2478/bjmg-2014-0021

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4347473/
https://www.ncbi.nlm.nih.gov/pubmed/25741211
http://dx.doi.org/10.2478/bjmg-2014-0021

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