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M Wehnert

Showing results (11-20 of 45) with videos related to

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Human Genetics|December 22, 1999
Identification, mapping, and genomic structure of a novel X-chromosomal human gene (SMPX) encoding a small muscular proteinD Patzak, O Zhuchenko, C C Lee, et al.
European Journal of Pediatrics|January 1, 1990
Deletion screening and prenatal diagnosis of Duchenne muscular dystrophy using cDNA probes Cf 23a and Cf 56aF H Herrmann, K Wulff, M Schütz, et al.
Cytogenetics and Cell Genetics|May 27, 1999
Genomic organization of the human complex I 13-kDa subunit gene NDUFA5K Tensing, I Pata, I Wittig, et al.
Journal of Neurology|December 1, 1989
Deletion screening in patients with Duchenne muscular dystrophyK Wulff, F H Herrmann, M C Wapenaar, et al.
Human Genetics|June 1, 1992
Structural gene aberrations in mucopolysaccharidosis II (Hunter)M Wehnert, J J Hopwood, W Schröder, et al.
Human Genetics|January 1, 1983
Reliability of the Tønnesen technique for the identification of Hunter carriersL Petruschka, G Machill, M Wehnert, et al.
Human Mutation|January 1, 1997
Six novel mutations in the emerin gene causing X-linked Emery-Dreifuss muscular dystrophyK Wulff, J E Parrish, F H Herrmann, et al.
Cytogenetics and Cell Genetics|February 22, 2002
Expression pattern and further characterization of human MAGED2 and identification of rodent orthologuesK Langnaese, D U Kloos, M Wehnert, et al.
Prenatal Diagnosis|June 1, 1989
Prenatal diagnosis of phenylketonuria by haplotype analysisK Wulff, M Wehnert, M Schütz, et al.
Haemostasis|September 1, 1996
Large-scale screening for factor V Leiden mutation in a north-eastern German populationW Schröder, M Koesling, K Wulff, et al.
Pageof 5

Showing results (11-20 of 45) with videos related to

Sort By:
Pageof 5
Human Genetics|December 22, 1999
Identification, mapping, and genomic structure of a novel X-chromosomal human gene (SMPX) encoding a small muscular proteinD Patzak, O Zhuchenko, C C Lee, et al.
European Journal of Pediatrics|January 1, 1990
Deletion screening and prenatal diagnosis of Duchenne muscular dystrophy using cDNA probes Cf 23a and Cf 56aF H Herrmann, K Wulff, M Schütz, et al.
Cytogenetics and Cell Genetics|May 27, 1999
Genomic organization of the human complex I 13-kDa subunit gene NDUFA5K Tensing, I Pata, I Wittig, et al.
Journal of Neurology|December 1, 1989
Deletion screening in patients with Duchenne muscular dystrophyK Wulff, F H Herrmann, M C Wapenaar, et al.
Human Genetics|June 1, 1992
Structural gene aberrations in mucopolysaccharidosis II (Hunter)M Wehnert, J J Hopwood, W Schröder, et al.
Human Genetics|January 1, 1983
Reliability of the Tønnesen technique for the identification of Hunter carriersL Petruschka, G Machill, M Wehnert, et al.
Human Mutation|January 1, 1997
Six novel mutations in the emerin gene causing X-linked Emery-Dreifuss muscular dystrophyK Wulff, J E Parrish, F H Herrmann, et al.
Cytogenetics and Cell Genetics|February 22, 2002
Expression pattern and further characterization of human MAGED2 and identification of rodent orthologuesK Langnaese, D U Kloos, M Wehnert, et al.
Prenatal Diagnosis|June 1, 1989
Prenatal diagnosis of phenylketonuria by haplotype analysisK Wulff, M Wehnert, M Schütz, et al.
Haemostasis|September 1, 1996
Large-scale screening for factor V Leiden mutation in a north-eastern German populationW Schröder, M Koesling, K Wulff, et al.
Pageof 5