Literature DB >> 4544175

Absence of measurable linkage between the loci for hypoxanthine-guanine phosphoribosyltransferase and deutan colorblindness.

B T Emmerson, L Thompson, D C Wallace, M A Spence.   

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Year:  1974        PMID: 4544175      PMCID: PMC1762560     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


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  12 in total

1.  A FAMILIAL DISORDER OF URIC ACID METABOLISM AND CENTRAL NERVOUS SYSTEM FUNCTION.

Authors:  M LESCH; W L NYHAN
Journal:  Am J Med       Date:  1964-04       Impact factor: 4.965

2.  HEREDITARY CHOREOATHETOSIS, SELF-MUTILATION AND HYPERURICEMIA IN YOUNG MALES.

Authors:  D HOEFNAGEL; E D ANDREW; N G MIREAULT; W O BERNDT
Journal:  N Engl J Med       Date:  1965-07-15       Impact factor: 91.245

3.  Genetical linkage between the loci for glucose-6-phosphate dehydrogenase deficiency and colour-blindness in American Negroes.

Authors:  I H PORTER; J SCHULZE; V A MCKUSICK
Journal:  Ann Hum Genet       Date:  1962-11       Impact factor: 1.670

Review 4.  Hypoxanthine-guanine phosphoribosyltransferase deficiency in gout.

Authors:  W N Kelley; M L Greene; F M Rosenbloom; J F Henderson; J E Seegmiller
Journal:  Ann Intern Med       Date:  1969-01       Impact factor: 25.391

5.  Linkage analysis in man by somatic cell genetics.

Authors:  F H Ruddle
Journal:  Nature       Date:  1973-03-16       Impact factor: 49.962

6.  The spectrum of hypoxanthine-guanine phosphoribosyltransferase deficiency.

Authors:  B T Emmerson; L Thompson
Journal:  Q J Med       Date:  1973-04

7.  Hypoxanthine-guanine phosphoribosyltransferase deficiency and Xg blood group.

Authors:  M L Greene; W L Nyhan; J E Seegmiller
Journal:  Am J Hum Genet       Date:  1970-01       Impact factor: 11.025

8.  Genetic studies of HG- PRT deficiency and the Lesch-Nyhan syndrome with cultured human cells.

Authors:  R DeMars
Journal:  Fed Proc       Date:  1971 May-Jun

9.  Partial deficiency of hypoxanthine-guanine phosphoribosyltransferase: intermediate enzyme deficiency in heterozygote red cells.

Authors:  B T Emmerson; D C Wallace; C J Thompson
Journal:  Ann Intern Med       Date:  1972-02       Impact factor: 25.391

10.  Hemizygous expression of glucose-6-phosphate dehydrogenase in erythrocytes of heterozygotes for the Lesch-Nyhan syndrome.

Authors:  W L Nyhan; B Bakay; J D Connor; J F Marks; D K Keele
Journal:  Proc Natl Acad Sci U S A       Date:  1970-01       Impact factor: 11.205

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  1 in total

1.  Identification of a single nucleotide substitution in the coding sequence of in vitro amplified cDNA from a patient with partial HPRT deficiency (HPRTBRISBANE).

Authors:  R B Gordon; D G Sculley; P A Dawson; I R Beacham; B T Emmerson
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

  1 in total

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