Normal view MARC view ISBD view

21-hydroxylase deficiency families with HLA identical affected and unaffected sibs.

Sinnott, P J

21-hydroxylase deficiency families with HLA identical affected and unaffected sibs. [electronic resource] - Journal of medical genetics Jan 1989 - 10-7 p. digital

Publication Type: Journal Article

ISSN: 0022-2593

Standard No.: 10.1136/jmg.26.1.10 doi

Subjects--Topical Terms:
Adrenal Hyperplasia, Congenital--genetics
Child
Chromosome Mapping
Complement C4--genetics
Female
HLA Antigens--genetics
HLA-B Antigens--genetics
Haplotypes
Humans
Pedigree
Steroid Hydroxylases--deficiency

Print
Cite
Add to your cart (remove)
Save record
BIBTEX Dublin Core MARCXML MARC (non-Unicode/MARC-8) MARC (Unicode/UTF-8) MARC (Unicode/UTF-8, Standard) MODS (XML) RIS ISBD
More searches

Search for this title in:
Other Libraries (WorldCat) Other Databases (Google Scholar) Online Stores (Bookfinder.com) Open Library (openlibrary.org)