Literature DB >> 2893183

Prenatal exclusion of primary hyperoxaluria type 1.

C J Danpure, P R Jennings, R J Penketh, P J Wise, C H Rodeck.   

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Year:  1988        PMID： 2893183     DOI： 10.1016/s0140-6736(88)91171-3

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  4 in total

Review 1.  Recent advances in the understanding, diagnosis and treatment of primary hyperoxaluria type 1.

Authors:  C J Danpure
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

2.  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

3.  [Type I oxalosis in childhood--studies within the scope of terminal renal failure in the child].

Authors:  M Frosch; E Kuwertz-Bröking; M Bulla; D B von Bassewitz; D B Leusmann
Journal:  Klin Wochenschr       Date:  1989-11-17

4.  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
  4 in total

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