Authors:
Webster, KE
Ferree, PM
Holmes, RP
Cramer, SD
Citation: Ke. Webster et al., Identification of missense, nonsense, and deletion mutations in the GRHPR gene in patients with primary hyperoxaluria type II (PH2), HUM GENET, 107(2), 2000, pp. 176-185
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Authors:
Cramer, SD
Ferree, PM
Lin, K
Milliner, DS
Holmes, RP
Citation: Sd. Cramer et al., The gene encoding hydroxypyruvate reductase (GRHPR) is mutated in patientswith primary hyperoxaluria type II (vol 8, pg 2063, 1999), HUM MOL GEN, 8(13), 1999, pp. 2574-2574
Authors:
Cramer, SD
Ferree, PM
Lin, K
Milliner, DS
Holmes, RP
Citation: Sd. Cramer et al., The gene encoding hydroxypyruvate reductase (GRHPR) is mutated in patientswith primary hyperoxaluria type II, HUM MOL GEN, 8(11), 1999, pp. 2063-2069
Authors:
Mann, SS
Hart, TC
Pettenati, MJ
von Kap-herr, C
Holmes, RP
Citation: Ss. Mann et al., Assignment of the sodium-dependent dicarboxylate transporter gene (SLC13A2alias NaDC-1) to human chromosome region 17p11.1 -> q11.1 by radiation hybrid mapping and fluorescence in situ hybridization, CYTOG C GEN, 84(1-2), 1999, pp. 89-90
Citation: H. Sidhu et al., Direct quantification of the enteric bacterium Oxalobacter formigenes in human fecal samples by quantitative competitive-template PCR, J CLIN MICR, 37(5), 1999, pp. 1503-1509
Citation: Rp. Holmes et al., A prospective study of maternal serum insulin-like growth factor-I in pregnancies with appropriately grown or growth restricted fetuses, BR J OBST G, 105(12), 1998, pp. 1273-1278