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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.

Detalles Bibliográficos
Autores principales:	Pokale, Yamini S., Jadhav, Ajinkya M., Kate, Ushang
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2012
Materias:	Case Report
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

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