Vol 8: A new mutation of the PCNT gene in a Colombian patient with microcephalic osteodysplastic primordial dwarfism type II: a case report.Reportar como inadecuado



 Vol 8: A new mutation of the PCNT gene in a Colombian patient with microcephalic osteodysplastic primordial dwarfism type II: a case report.


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This article is from Journal of Medical Case Reports, volume 8.AbstractIntroduction: Microcephalic osteodysplastic primordial dwarfism is a syndrome characterized by the presence of intrauterine growth restriction, post-natal growth deficiency and microcephaly. Microcephalic osteodysplastic primordial dwarfism type II is the most distinctive syndro

Autor: Pachajoa, Harry; Ruiz-Botero, Felipe; Isaza, Carolina

Fuente: https://archive.org/







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