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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.
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Medknow Publications & Media Pvt Ltd
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3385166/ https://ncbi.nlm.nih.gov/pubmed/22754235 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-6866.96677 |
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