Mapping of a single locus capable of complementing the defective heterochromatin phenotype of Roberts syndrome cells.

McDaniel, Lisa D

Mapping of a single locus capable of complementing the defective heterochromatin phenotype of Roberts syndrome cells. [electronic resource] - American journal of human genetics Jul 2005 - 132-9 p. digital

Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, P.H.S.

0002-9297

10.1086/431328 doi


Abnormalities, Multiple--genetics
Bone Diseases, Developmental--genetics
Chromosome Mapping
Chromosomes, Human, Pair 8
Craniofacial Abnormalities
Genetic Complementation Test
Heterochromatin--genetics
Homozygote
Humans
Phenotype
Syndrome