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E Rötzer

Showing results (1-10 of 5) with videos related to

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European Journal of Medical Research|April 29, 1998
Rapid DNA extraction method for genetic screeningM Gross, E Rötzer
Advances in Experimental Medicine and Biology|May 23, 1998
The genetic basis of myoadenylate deaminase deficiency is heterogeneousE Rötzer, W Mortier, H Reichmann, et al.
Human Mutation|January 1, 1995
Identification of a new missense mutation in exon 2 of the human hypoxanthine phosphoribosyltransferase gene (HPRTIsar): a further example of clinical heterogeneity in HPRT deficienciesR Burgemeister, E Rötzer, W Gutensohn, et al.
Human Heredity|January 1, 1992
Leber's hereditary optic neuroretinopathy and the X-chromosomal susceptibility factor: no linkage to DXs7M R Carvalho, B Müller, E Rötzer, et al.
Neuromuscular Disorders : NMD|July 16, 2002
A G468-T AMPD1 mutant allele contributes to the high incidence of myoadenylate deaminase deficiency in the Caucasian populationM Gross, E Rötzer, P Kölle, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
European Journal of Medical Research|April 29, 1998
Rapid DNA extraction method for genetic screeningM Gross, E Rötzer
Advances in Experimental Medicine and Biology|May 23, 1998
The genetic basis of myoadenylate deaminase deficiency is heterogeneousE Rötzer, W Mortier, H Reichmann, et al.
Human Mutation|January 1, 1995
Identification of a new missense mutation in exon 2 of the human hypoxanthine phosphoribosyltransferase gene (HPRTIsar): a further example of clinical heterogeneity in HPRT deficienciesR Burgemeister, E Rötzer, W Gutensohn, et al.
Human Heredity|January 1, 1992
Leber's hereditary optic neuroretinopathy and the X-chromosomal susceptibility factor: no linkage to DXs7M R Carvalho, B Müller, E Rötzer, et al.
Neuromuscular Disorders : NMD|July 16, 2002
A G468-T AMPD1 mutant allele contributes to the high incidence of myoadenylate deaminase deficiency in the Caucasian populationM Gross, E Rötzer, P Kölle, et al.
Pageof 1