TY  - GEN
AU  - Potocki,L
AU  - Chen,K S
AU  - Park,S S
AU  - Osterholm,D E
AU  - Withers,M A
AU  - Kimonis,V
AU  - Summers,A M
AU  - Meschino,W S
AU  - Anyane-Yeboa,K
AU  - Kashork,C D
AU  - Shaffer,L G
AU  - Lupski,J R
TI  - Molecular mechanism for duplication 17p11.2- the homologous recombination reciprocal of the Smith-Magenis microdeletion
SN  - 1061-4036
PY  - 2000///0210
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Chromosome Aberrations
KW  - Chromosomes, Human, Pair 17
KW  - Female
KW  - Genotype
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Intellectual Disability
KW  - Male
KW  - Pedigree
KW  - Recombination, Genetic
KW  - Syndrome
N1  - Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1038/71743
ER  -