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Phenotypical characterization of 13q deletion syndrome: Report of two cases

Patients with 13q deletion syndrome are characterized with different phenotypical features depending on the size and location of the deleted region on chromosome 13. These patients fall into three groups: In Group 1, deleted region is in the proximal and does not extend into q32; in Group 2, deleted...

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Detalles Bibliográficos
Autores principales:	Bagherizadeh, Eiman, Shafaghati, Yousef, Hadipour, Fatemeh, Behjati, Farkhondeh
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2014
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4228577/ https://www.ncbi.nlm.nih.gov/pubmed/25400354 http://dx.doi.org/10.4103/0971-6866.142912

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