Literature DB >> 5980574

X-linked recessive inheritance of a syndrome of mental retardation with hyperuricemia.

S L Shapiro, G L Sheppard, F E Dreifuss, D S Newcombe.   

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Year:  1966        PMID: 5980574     DOI: 10.3181/00379727-122-31204

Source DB:  PubMed          Journal:  Proc Soc Exp Biol Med        ISSN: 0037-9727


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  16 in total

Review 1.  Pathophysiology of hyperuricemia in primary gout.

Authors:  J B Wyngaarden
Journal:  Trans Am Clin Climatol Assoc       Date:  1970

2.  A specific enzyme defect in gout associated with overproduction of uric acid.

Authors:  W N Kelley; F M Rosenbloom; J F Henderson; J E Seegmiller
Journal:  Proc Natl Acad Sci U S A       Date:  1967-06       Impact factor: 11.205

3.  Mosaicism of peripheral blood lymphocyte populations in females heterozygous for the Lesch-Nyhan mutation.

Authors:  R J Albertini; R DeMars
Journal:  Biochem Genet       Date:  1974-05       Impact factor: 1.890

4.  [Lesch-Nyhan syndrome. Heterozygote detection by biochemical selection of the mutant cells and autoradiography].

Authors:  A M Hagemeijer; P Dodinval; J M Andrien
Journal:  Humangenetik       Date:  1972

5.  Juvenile gout.

Authors:  B L Treadwell
Journal:  Ann Rheum Dis       Date:  1971-05       Impact factor: 19.103

6.  [Observations on the problem of sex-linked recessive mental retardation].

Authors:  G Neuhäuser; E Zerbin-Rüdin; R A Pfeiffer; H Klar
Journal:  Arch Psychiatr Nervenkr (1970)       Date:  1969

7.  X-chromosome inactivation and the Xg locus.

Authors:  P J Fialkow
Journal:  Am J Hum Genet       Date:  1970-07       Impact factor: 11.025

8.  An electrophoretic method for detecting hypoxanthine-guanine phosphoribosyl transferase variants.

Authors:  V M Der Kaloustian; R Byrne; W J Young; B Childs
Journal:  Biochem Genet       Date:  1969-06       Impact factor: 1.890

9.  Inheritance of purine phosphoribosyltransferases in man.

Authors:  J F Henderson; W N Kelley; F M Rosenbloom; J E Seegmiller
Journal:  Am J Hum Genet       Date:  1969-01       Impact factor: 11.025

Review 10.  Hypoxanthine-guanine phosphoribosyl transferase deficiency.

Authors:  C H de Bruyn
Journal:  Hum Genet       Date:  1976-02-29       Impact factor: 4.132

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