Literature DB >> 5816967

A method for the prenatal diagnosis of congenital hyperuricemia.

P H Berman, M E Balis, J Dancis.   

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Year:  1969        PMID： 5816967     DOI： 10.1016/s0022-3476(69)80279-9

Source DB:  PubMed          Journal:  J Pediatr        ISSN： 0022-3476            Impact factor:   4.406


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  4 in total

1.  [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

2.  Cell population density and phenotypic expression of tissue culture fibroblasts from heterozygotes of Lesch-Nyhan's disease (inosinate pyrophosphorylase deficiency).

Authors:  J Dancis; R P Cox; P H Berman; V Jansen; M E Balis
Journal:  Biochem Genet       Date:  1969-12       Impact factor: 1.890

3.  The use of amniocentesis for prenatal genetic counseling.

Authors:  M Gertner; L Y Hsu; J Martin; K Hirshhorn
Journal:  Bull N Y Acad Med       Date:  1970-11

4.  Evidence for transfer of enzyme product as the basis of metabolic cooperation between tissue culture fibroblasts of Lesch-Nyhan disease and normal cells.

Authors:  R P Cox; M R Krauss; M E Balis; J Dancis
Journal:  Proc Natl Acad Sci U S A       Date:  1970-11       Impact factor: 11.205
  4 in total

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