KBG syndrome involving a single-nucleotide duplication in ANKRD11

KBG syndrome is a rare autosomal dominant genetic condition characterized by neurological involvement and distinct facial, hand, and skeletal features. More than 70 cases have been reported; however, it is likely that KBG syndrome is underdiagnosed because of lack of comprehensive characterization o...

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Detalles Bibliográficos
Autores principales: Kleyner, Robert, Malcolmson, Janet, Tegay, David, Ward, Kenneth, Maughan, Annette, Maughan, Glenn, Nelson, Lesa, Wang, Kai, Robison, Reid, Lyon, Gholson J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2016
Materias:
Research Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5111005/
https://www.ncbi.nlm.nih.gov/pubmed/27900361
http://dx.doi.org/10.1101/mcs.a001131

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5111005/
https://www.ncbi.nlm.nih.gov/pubmed/27900361
http://dx.doi.org/10.1101/mcs.a001131

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