TY  - GEN
AU  - Grau,Christina
AU  - Starkovich,Molly
AU  - Azamian,Mahshid S
AU  - Xia,Fan
AU  - Cheung,Sau Wai
AU  - Evans,Patricia
AU  - Henderson,Alex
AU  - Lalani,Seema R
AU  - Scott,Daryl A
TI  - Xp11.22 deletions encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a cause of syndromic X-linked intellectual disability
SN  - 1932-6203
PY  - 2017///0424
KW  - Antigens, Neoplasm
KW  - genetics
KW  - Child
KW  - Child, Preschool
KW  - Chromosomal Proteins, Non-Histone
KW  - Chromosome Duplication
KW  - Chromosomes, Human, X
KW  - Comparative Genomic Hybridization
KW  - methods
KW  - Developmental Disabilities
KW  - Female
KW  - Genes, X-Linked
KW  - Humans
KW  - Intellectual Disability
KW  - Male
KW  - Neoplasm Proteins
KW  - Pedigree
KW  - Peptide Termination Factors
KW  - Phenotype
KW  - Sequence Deletion
KW  - X Chromosome Inactivation
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1371/journal.pone.0175962
ER  -