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Case Reports

. 1988 Feb 13;1(8581):367.

doi: 10.1016/s0140-6736(88)91171-3.

Prenatal exclusion of primary hyperoxaluria type 1

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

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

Case Reports

Prenatal exclusion of primary hyperoxaluria type 1

C J Danpure et al. Lancet. 1988.

. 1988 Feb 13;1(8581):367.

doi: 10.1016/s0140-6736(88)91171-3.

Authors

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

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

No abstract available

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Molecular characterization and clinical use of a polymorphic tandem repeat in an intron of the human alanine:glyoxylate aminotransferase gene.
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Recent advances in the understanding, diagnosis and treatment of primary hyperoxaluria type 1.
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