Hypoxanthine-guanine phosphoribosyltransferase deficiency and Xg blood group.

American journal of human genetics ·Vol. 22 ·No. 1 ·1970-01-00 ·Pages 50-4

Greene ML, Nyhan WL, Seegmiller JE

Abstract

暂无摘要

MeSH Terms

Blood Group Antigens Chromosome Mapping Female Heterozygote Humans Hypoxanthines Male Pedigree Pentosephosphates Purine-Pyrimidine Metabolism, Inborn Errors/genetics Recombination, Genetic Transferases/metabolism Vision Tests

Chemicals

Blood Group Antigens Hypoxanthines Pentosephosphates Transferases

Authors & Affiliations

3 authors, click to expand affiliations / ORCID

Greene M L

Nyhan W L

Seegmiller J E

References (21)

21 references, click to expand

The Xg blood groups and congenital hypogammaglobulinemia.
Vox Sang. 1965 Nov-Dec;10(6):729-30 PMID: 5860323
A common X-linked serum marker and its relation to other loci on the X chromosome.
Trans Assoc Am Physicians. 1966;79:165-76 PMID: 5929457
A specific enzyme defect in gout associated with overproduction of uric acid.
Proc Natl Acad Sci U S A. 1967 Jun;57(6):1735-9 PMID: 4291947
Inherited disorder of purine metabolism. Correlation between central nervous system dysfunction and biochemical defects.
JAMA. 1967 Oct 16;202(3):175-7 PMID: 6072350
Deletion of the long arm of chromosome 16 and an unexpected Duffy blood group phenotype reveal a possible autosomal linkage.
Nature. 1967 Sep 2;215(5105):1075-6 PMID: 6053430
Ocular albinism and Xg.
Lancet. 1968 Jun 15;1(7555):1282-3 PMID: 4172140
Possible localisation of the gene for cystic fibrosis of the pancreas to the short arm of chromosome 5.
Lancet. 1968 Aug 10;2(7563):309-12 PMID: 4173733
Prenatal detection of genetic defects.
J Pediatr. 1969 Jan;74(1):132-43 PMID: 4882540
A new disorder of purine metabolism with behavioral manifestations.
J Pediatr. 1969 Jan;74(1):20-7 PMID: 5782823
Further data from Greece on recombination between the Xg blood group and glucose-6-phosphate dehydrogenase deficiency.
Am J Hum Genet. 1968 Nov;20(6):528-33 PMID: 5703688
Inheritance of purine phosphoribosyltransferases in man.
Am J Hum Genet. 1969 Jan;21(1):61-70 PMID: 5763607
Hypoxanthine-guanine phosphoribosyltransferase deficiency in gout.
Ann Intern Med. 1969 Jan;70(1):155-206 PMID: 4884382
A tetrazolium method for distinguishing between cultured human fibroblasts having eiter normal or deficient levels of glucose-6-phosphate dehydrogenase.
Biochem Genet. 1967 Jun;1(1):61-4 PMID: 5610701
The linkage relations of the loci for benign (Becker type) X-borne muscular dystrophy, colour blindness and the Xg blood groups.
Ann Hum Genet. 1969 Jan;32(3):261-9 PMID: 5305175
Linkage relations of X-borne ichthyosis to the Xg blood groups and to other markers of the X in Israelis.
Ann Hum Genet. 1969 May;32(4):323-32 PMID: 5307230
X-linked ichthyosis: linkage relationship with the Xg blood groups and other studies in a large Dutch kindred.
Ann Hum Genet. 1969 May;32(4):333-45 PMID: 5307231
Linkage relationships of the angiokeratoma (Fabry) locus.
Ann Hum Genet. 1969 May;32(4):369-74 PMID: 5307232
THE LINKAGE RELATIONS OF HEMOPHILIA A AND HEMOPHILIA B (CHRISTMAS DISEASE) TO THE XG BLOOD GROUP SYSTEM.
Am J Hum Genet. 1963 Dec;15:481-92 PMID: 14097242
A FAMILIAL DISORDER OF URIC ACID METABOLISM AND CENTRAL NERVOUS SYSTEM FUNCTION.
Am J Med. 1964 Apr;36:561-70 PMID: 14142409
X CHROMOSOME MAPPING OF GENES FOR RED-GREEN COLORBLINDNESS AND XG.
Am J Hum Genet. 1964 Dec;16:403-9 PMID: 14250421
HEREDITARY CHOREOATHETOSIS, SELF-MUTILATION AND HYPERURICEMIA IN YOUNG MALES.
N Engl J Med. 1965 Jul 15;273:130-5 PMID: 14303658

Article Info

Journal

American journal of human genetics

Abbr.

Am J Hum Genet

ISSN

0002-9297

Published

1970-01-00

Pages

50-4

Language

English

Region

United States

NLM ID

0370475

PMCID

PMC1706515

Subset

External Links

PubMed source PMC Full Text View journal details

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Hypoxanthine-guanine phosphoribosyltransferase deficiency and Xg blood group.

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