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Trichorhinophalangeal syndrome type 1: A case report with literature review

Trichorhinophalangeal syndrome is a very rare genetic disorder, where damage and mutation to the number 8 chromosome affects sufferers in numerous ways. The syndrome has three types, all characterized by abnormally short stature, sparse hair, short deformed fingers with cone-shaped epiphyses visible...

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Detalles Bibliográficos
Autores principales:	Candamourty, Ramesh, Venkatachalam, Suresh, Karthikeyan, B., Babu, M. R. Ramesh
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/PMC3510923/ https://www.ncbi.nlm.nih.gov/pubmed/23225991 http://dx.doi.org/10.4103/0976-9668.101936

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