Terminal osseous dysplasia with pigmentary defects maps to human chromosome Xq27.3-xqter. [electronic resource]
Producer: 20000531Description: 1461-4 p. digitalISSN:- 0002-9297
- Abnormalities, Multiple -- genetics
- Bone Diseases, Developmental -- genetics
- Chromosome Mapping
- DNA Methylation
- Dosage Compensation, Genetic
- Female
- Genetic Linkage -- genetics
- Haplotypes -- genetics
- Humans
- Infant, Newborn
- Lod Score
- Male
- Pedigree
- Pigmentation Disorders -- genetics
- Polymorphism, Genetic -- genetics
- Recombination, Genetic
- X Chromosome -- genetics
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
There are no comments on this title.
Log in to your account to post a comment.