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Results:
1-7
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Results: 7
Authors:
VONSCHNAKENBURG C
RUMSBY G
Citation: C. Vonschnakenburg et G. Rumsby, IDENTIFICATION OF NEW MUTATIONS IN PRIMARY HYPEROXALURIA TYPE-1 (PH1), JN. Journal of nephrology, 11, 1998, pp. 15-17
Authors:
VONSCHNAKENBURG C
HULTON SA
MILFORD DV
ROPER HP
RUMSBY G
Citation: C. Vonschnakenburg et al., VARIABLE PRESENTATION OF PRIMARY HYPEROXALURIA TYPE-1 IN 2 PATIENTS HOMOZYGOUS FOR A NOVEL COMBINED DELETION AND INSERTION MUTATION IN EXON-8 OF THE AGXT GENE, Nephron, 78(4), 1998, pp. 485-488
Authors:
TARN AC
VONSCHNAKENBURG C
RUMSBY G
Citation: Ac. Tarn et al., PRIMARY HYPEROXALURIA TYPE-1 - DIAGNOSTIC RELEVANCE OF MUTATIONS AND POLYMORPHISMS IN THE ALANINE-GLYOXYLATE AMINOTRANSFERASE GENE (AGXT), Journal of inherited metabolic disease, 20(5), 1997, pp. 689-696
Authors:
VONSCHNAKENBURG C
HOYER PF
LATTA K
SCHLITT HJ
OFFNER G
Citation: C. Vonschnakenburg et al., LETHAL COURSE OF VARICELLA AFTER KIDNEY-T RANSPLANTATION, Monatsschrift fur Kinderheilkunde, 145(2), 1997, pp. 114-116
Authors:
VONSCHNAKENBURG C
RUMSBY G
Citation: C. Vonschnakenburg et G. Rumsby, PRIMARY HYPEROXALURIA TYPE-1 - A CLUSTER OF NEW MUTATIONS IN EXON-7 OF THE AGXT-GENE, Journal of Medical Genetics, 34(6), 1997, pp. 489-492
Authors:
VONSCHNAKENBURG C
WEIR T
RUMSBY G
Citation: C. Vonschnakenburg et al., LINKAGE OF MICROSATELLITES TO THE AGXT GENE ON CHROMOSOME 2Q37.3 AND THEIR ROLE IN PRENATAL-DIAGNOSIS OF PRIMARY HYPEROXALURIA TYPE-1, Annals of Human Genetics, 61, 1997, pp. 365-368
Authors:
VONSCHNAKENBURG C
BYRD DJ
LATTA K
REUSZ GS
GRAF D
BRODEHL J
Citation: C. Vonschnakenburg et al., DETERMINATION OF OXALATE EXCRETION IN SPOT URINES OF HEALTHY-CHILDRENBY ION CHROMATOGRAPHY, European journal of clinical chemistry and clinical biochemistry, 32(1), 1994, pp. 27-29
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1-7
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