TY  - GEN
AU  - Zhang,W
AU  - Amir,R
AU  - Stockton,D W
AU  - Van Den Veyver,I B
AU  - Bacino,C A
AU  - Zoghbi,H Y
TI  - Terminal osseous dysplasia with pigmentary defects maps to human chromosome Xq27.3-xqter
SN  - 0002-9297
PY  - 2000///0531
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Bone Diseases, Developmental
KW  - Chromosome Mapping
KW  - DNA Methylation
KW  - Dosage Compensation, Genetic
KW  - Female
KW  - Genetic Linkage
KW  - Haplotypes
KW  - Humans
KW  - Infant, Newborn
KW  - Lod Score
KW  - Male
KW  - Pedigree
KW  - Pigmentation Disorders
KW  - Polymorphism, Genetic
KW  - Recombination, Genetic
KW  - X Chromosome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1086/302868
ER  -