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European Journal of Obstetrics, Gynecology, and Reproductive Biology|July 14, 2001
Combined heterozygosity for methylenetetrahydrofolate reductase (MTHFR) mutations C677T and A1298C is associated with abruptio placentae but not with intrauterine growth restrictionG S Gebhardt, C L Scholtz, R Hillermann, et al.
Human Molecular Genetics|July 13, 1999
Spectrum of mutations in the HFE gene implicated in haemochromatosis and porphyriaJ N de Villiers, R Hillermann, L Loubser, et al.
Human Genetics|December 1, 1995
Human glial cell line-derived neurotrophic factor (GDNF) maps to chromosome 5N Bermingham, R Hillermann, F Gilmour, et al.
Placenta|December 7, 2007
Prediction of preeclampsia - a workshop reportN G Than, R Romero, R Hillermann, et al.
Genetic Counseling (Geneva, Switzerland)|August 9, 2001
Prenatal diagnosis of familial hypercholesterolemia: importance of DNA analysis in the high-risk South African populationJ Vergotine, R Thiart, E Langenhoven, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Physical evidence for the position of the Friedreich's ataxia locus FRDA proximal to D9S5R Hillermann, C G See, M Pook, et al.
Human Molecular Genetics|August 1, 1995
Friedreich's ataxia: a defect in signal transduction?J J Carvajal, M A Pook, K Doudney, et al.
Nature Genetics|October 1, 1996
The Friedreich's ataxia gene encodes a novel phosphatidylinositol-4- phosphate 5-kinaseJ J Carvajal, M A Pook, M dos Santos, et al.
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