TY  - GEN
AU  - Froyen,Guy
AU  - Bauters,Marijke
AU  - Boyle,Jackie
AU  - Van Esch,Hilde
AU  - Govaerts,Karen
AU  - van Bokhoven,Hans
AU  - Ropers,Hans-Hilger
AU  - Moraine,Claude
AU  - Chelly,Jamel
AU  - Fryns,Jean-Pierre
AU  - Marynen,Peter
AU  - Gecz,Jozef
AU  - Turner,Gillian
TI  - 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
SN  - 0340-6717
PY  - 2007///1010
KW  - Amino Acid Transport Systems, Neutral
KW  - genetics
KW  - Chromosome Deletion
KW  - Chromosomes, Human, X
KW  - Female
KW  - Humans
KW  - Intellectual Disability
KW  - Male
KW  - Methyltransferases
KW  - Nuclear Proteins
KW  - Polymerase Chain Reaction
KW  - Sex Chromosome Aberrations
KW  - Siblings
KW  - X Chromosome Inactivation
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1007/s00439-007-0343-1
ER  -