TY  - GEN
AU  - Duker,Angela L
AU  - Ballif,Blake C
AU  - Bawle,Erawati V
AU  - Person,Richard E
AU  - Mahadevan,Sangeetha
AU  - Alliman,Sarah
AU  - Thompson,Regina
AU  - Traylor,Ryan
AU  - Bejjani,Bassem A
AU  - Shaffer,Lisa G
AU  - Rosenfeld,Jill A
AU  - Lamb,Allen N
AU  - Sahoo,Trilochan
TI  - Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome
SN  - 1476-5438
PY  - 2011///0302
KW  - Base Sequence
KW  - Child
KW  - Chromosome Breakpoints
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 15
KW  - genetics
KW  - Comparative Genomic Hybridization
KW  - Fathers
KW  - Genotype
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Male
KW  - Multigene Family
KW  - Phenotype
KW  - Polymorphism, Single Nucleotide
KW  - Prader-Willi Syndrome
KW  - RNA, Small Nucleolar
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1038/ejhg.2010.102
ER  -