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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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| Publicado no: | Balkan J Med Genet |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Macedonian Science of Sciences and Arts
2014
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| 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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