A catalog of hemizygous variation in 127 22q11 deletion patients

The 22q11.2 deletion syndrome is the most common microdeletion disorder, with wide phenotypic variability. To investigate variation within the non-deleted allele we performed targeted resequencing of the 22q11.2 region for 127 patients, identifying multiple deletion sizes, including two deletions wi...

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Detalles Bibliográficos
Autores principales: Hestand, Matthew S, Nowakowska, Beata A, Vergaelen, Elfi, Van Houdt, Jeroen, Dehaspe, Luc, Suhl, Joshua A, Del-Favero, Jurgen, Mortier, Geert, Zackai, Elaine, Swillen, Ann, Devriendt, Koenraad, Gur, Raquel E, McDonald-McGinn, Donna M, Warren, Stephen T, Emanuel, Beverly S, Vermeesch, Joris R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892188/
https://www.ncbi.nlm.nih.gov/pubmed/27274857
http://dx.doi.org/10.1038/hgv.2015.65

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892188/
https://www.ncbi.nlm.nih.gov/pubmed/27274857
http://dx.doi.org/10.1038/hgv.2015.65

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