Literature DB >> 8703709

What are the present possibilities for the prenatal diagnosis of primary hyperoxaluria?

C J Danpure1.   

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Year:  1996        PMID： 8703709     DOI： 10.1007/BF00862073

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN： 0931-041X            Impact factor:   3.714


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  5 in total

1.  Enzymatic prenatal diagnosis of primary hyperoxaluria type 1: potential and limitations.

Authors:  C J Danpure; P J Cooper; P R Jennings; P J Wise; R J Penketh; C H Rodeck
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

2.  Fetal liver alanine: glyoxylate aminotransferase and the prenatal diagnosis of primary hyperoxaluria type 1.

Authors:  C J Danpure; P R Jennings; R J Penketh; P J Wise; P J Cooper; C H Rodeck
Journal:  Prenat Diagn       Date:  1989-04       Impact factor: 3.050

3.  Molecular characterization and clinical use of a polymorphic tandem repeat in an intron of the human alanine:glyoxylate aminotransferase gene.

Authors:  C J Danpure; G M Birdsey; G Rumsby; M J Lumb; P E Purdue; J Allsop
Journal:  Hum Genet       Date:  1994-07       Impact factor: 4.132

Review 4.  Primary hyperoxaluria type 1: genotypic and phenotypic heterogeneity.

Authors:  C J Danpure; P R Jennings; P Fryer; P E Purdue; J Allsop
Journal:  J Inherit Metab Dis       Date:  1994       Impact factor: 4.982

5.  An intronic duplication in the alanine: glyoxylate aminotransferase gene facilitates identification of mutations in compound heterozygote patients with primary hyperoxaluria type 1.

Authors:  P E Purdue; M J Lumb; J Allsop; C J Danpure
Journal:  Hum Genet       Date:  1991-08       Impact factor: 4.132
  5 in total

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