TY  - GEN
AU  - McDaniel,Lisa D
AU  - Tomkins,Darrell J
AU  - Stanbridge,Eric J
AU  - Somerville,Martin J
AU  - Friedberg,Errol C
AU  - Schultz,Roger A
TI  - Mapping of a single locus capable of complementing the defective heterochromatin phenotype of Roberts syndrome cells
SN  - 0002-9297
PY  - 2005///0829
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Bone Diseases, Developmental
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 8
KW  - Craniofacial Abnormalities
KW  - Genetic Complementation Test
KW  - Heterochromatin
KW  - Homozygote
KW  - Humans
KW  - Phenotype
KW  - Syndrome
N1  - Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1086/431328
ER  -