Strategies for the prenatal diagnosis of primary hyperoxaluria type 1

Prenatal Diagnosis

Volumn 16, Issue 7, 1996, Pages 587-598

  Danpure, Christopher J ^a   Rumsby, Gillian ^b  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b ROYAL FREE AND UNIVERSITY COLLEGE MEDICAL SCHOOL   (United Kingdom)

Author keywords

AGXT gene; Alanine:glyoxylate aminotransferase; Primary hyperoxaluria type 1

Indexed keywords

ALANINE GLYOXYLATE AMINOTRANSFERASE; GLYOXYLIC ACID;

AMNION FLUID; AUTOSOMAL DOMINANT INHERITANCE; CHORION VILLUS; DIAGNOSTIC VALUE; DNA DETERMINATION; ENZYME ASSAY; ENZYME DEFICIENCY; FETUS; FETUS LIVER; FIRST TRIMESTER PREGNANCY; GENE MUTATION; GENETIC LINKAGE; HUMAN; IMMUNOASSAY; IMMUNOELECTRON MICROSCOPY; INBORN ERROR OF METABOLISM; INTERMETHOD COMPARISON; LIVER BIOPSY; METHODOLOGY; OXALOSIS 1; PATHOGENESIS; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; REVIEW; SECOND TRIMESTER PREGNANCY;

ALLELES; FEMALE; FETAL DISEASES; HUMANS; HYPEROXALURIA, PRIMARY; LINKAGE (GENETICS); LIVER; MALE; POINT MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, GENETIC; PREGNANCY; PRENATAL DIAGNOSIS; TRANSAMINASES;

EID: 0029898180     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199607)16:7<587::AID-PD925>3.0.CO;2-9     Document Type: Review

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