Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region

Author: Froyen Guy   Bauters Marijke   Boyle Jackie   Esch Hilde   Govaerts Karen   Bokhoven Hans   Ropers Hans-Hilger   Moraine Claude   Chelly Jamel   Fryns Jean-Pierre   Marynen Peter   Gecz Jozef   Turner Gillian  

Publisher: Springer Publishing Company

ISSN: 0340-6717

Source: Human Genetics, Vol.121, Iss.5, 2007-06, pp. : 539-547

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Related content