Submicroscopic copy-number variations associated with 46,XY disorders of sex development

BACKGROUND: Mutations in known causative genes and cytogenetically detectable chromosomal rearrangements account for a fraction of cases with 46,XY disorders of sex development (DSD). Recent advances in molecular cytogenetic technologies, including array-based comparative genomic hybridization (aCGH...

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Detalles Bibliográficos
Autores principales: Kon, Masafumi, Fukami, Maki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2015
Materias:
Mini Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4530572/
https://www.ncbi.nlm.nih.gov/pubmed/26542297
http://dx.doi.org/10.1186/s40348-015-0018-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4530572/
https://www.ncbi.nlm.nih.gov/pubmed/26542297
http://dx.doi.org/10.1186/s40348-015-0018-2

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