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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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Detalhes bibliográficos
Publicado no:Indian J Hum Genet
Main Authors: Bagherizadeh, Eiman, Shafaghati, Yousef, Hadipour, Fatemeh, Behjati, Farkhondeh
Formato: Artigo
Idioma:Inglês
Publicado em: Medknow Publications & Media Pvt Ltd 2014
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4228577/
https://ncbi.nlm.nih.gov/pubmed/25400354
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0971-6866.142912
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