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Wolf–Hirschhorn syndrome: A case demonstrated by a cytogenetic study
We present a case with a 4p terminal deletion, evidenced in GTG-banded chromosome study. Phenotypic signs described in the classical Wolf–Hirschhorn syndrome were found on clinical examination of our patient.
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3385166/ https://www.ncbi.nlm.nih.gov/pubmed/22754235 http://dx.doi.org/10.4103/0971-6866.96677 |