TY  - GEN
AU  - Whibley,Annabel C
AU  - Plagnol,Vincent
AU  - Tarpey,Patrick S
AU  - Abidi,Fatima
AU  - Fullston,Tod
AU  - Choma,Maja K
AU  - Boucher,Catherine A
AU  - Shepherd,Lorraine
AU  - Willatt,Lionel
AU  - Parkin,Georgina
AU  - Smith,Raffaella
AU  - Futreal,P Andrew
AU  - Shaw,Marie
AU  - Boyle,Jackie
AU  - Licata,Andrea
AU  - Skinner,Cindy
AU  - Stevenson,Roger E
AU  - Turner,Gillian
AU  - Field,Michael
AU  - Hackett,Anna
AU  - Schwartz,Charles E
AU  - Gecz,Jozef
AU  - Stratton,Michael R
AU  - Raymond,F Lucy
TI  - Fine-scale survey of X chromosome copy number variants and indels underlying intellectual disability
SN  - 1537-6605
PY  - 2010///0901
KW  - Chromosome Breakage
KW  - Chromosome Segregation
KW  - genetics
KW  - Chromosomes, Human, X
KW  - Cohort Studies
KW  - DNA Copy Number Variations
KW  - Disease
KW  - Female
KW  - Gene Rearrangement
KW  - Genes, X-Linked
KW  - Humans
KW  - INDEL Mutation
KW  - Intellectual Disability
KW  - Male
KW  - Oligonucleotide Array Sequence Analysis
KW  - Pedigree
KW  - Reproducibility of Results
KW  - Retroelements
KW  - Sequence Deletion
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.ajhg.2010.06.017
ER  -