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S Schwemmle

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

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International Journal of Cancer|May 8, 2000
Genomic structure and mutation screening of the E2F4 gene in human tumorsS Schwemmle, G P Pfeifer
Human Genetics|August 1, 1989
How does inactivation change timing of replication in the human X chromosome?S Schwemmle, K Mehnert, W Vogel
American Journal of Human Genetics|April 16, 1998
The DMPK gene of severely affected myotonic dystrophy patients is hypermethylated proximal to the largely expanded CTG repeatP Steinbach, D Gläser, W Vogel, et al.
American Journal of Medical Genetics|January 11, 1996
X/autosome translocation in three generations ascertained through an infant with trisomy 16p due to failure of spreading of X-inactivationW Preis, G Barbi, S Liptay, et al.
Human Molecular Genetics|July 1, 1995
Heterogeneity of DM kinase repeat expansion in different fetal tissues and further expansion during cell proliferation in vitro: evidence for a casual involvement of methyl-directed DNA mismatch repair in triplet repeat stabilityD Wöhrle, I Kennerknecht, M Wolf, et al.
Journal of Immunogenetics|August 1, 1989
Organization of the AKR Qa region: structure of a divergent class I sequence, Q5kE H Weiss, D Bevec, G Messer, et al.
Immunogenetics|January 1, 1991
Developmental and tissue-specific expression of the Q5k geneS Schwemmle, D Bevec, G Brem, et al.
American Journal of Medical Genetics|June 27, 1997
XX-agonadism in a fetus with multiple dysraphic lesions: a new syndromeI Kennerknecht, T Mattfeldt, W Paulus, et al.
Genomics|July 1, 1993
Multipoint mapping of the central core disease locusS Schwemmle, K Wolff, L M Palmucci, et al.
American Journal of Human Genetics|June 1, 1997
Characterization of FMR1 promoter elements by in vivo-footprinting analysisS Schwemmle, E de Graaff, H Deissler, et al.
Pageof 1

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

Sort By:
Pageof 1
International Journal of Cancer|May 8, 2000
Genomic structure and mutation screening of the E2F4 gene in human tumorsS Schwemmle, G P Pfeifer
Human Genetics|August 1, 1989
How does inactivation change timing of replication in the human X chromosome?S Schwemmle, K Mehnert, W Vogel
American Journal of Human Genetics|April 16, 1998
The DMPK gene of severely affected myotonic dystrophy patients is hypermethylated proximal to the largely expanded CTG repeatP Steinbach, D Gläser, W Vogel, et al.
American Journal of Medical Genetics|January 11, 1996
X/autosome translocation in three generations ascertained through an infant with trisomy 16p due to failure of spreading of X-inactivationW Preis, G Barbi, S Liptay, et al.
Human Molecular Genetics|July 1, 1995
Heterogeneity of DM kinase repeat expansion in different fetal tissues and further expansion during cell proliferation in vitro: evidence for a casual involvement of methyl-directed DNA mismatch repair in triplet repeat stabilityD Wöhrle, I Kennerknecht, M Wolf, et al.
Journal of Immunogenetics|August 1, 1989
Organization of the AKR Qa region: structure of a divergent class I sequence, Q5kE H Weiss, D Bevec, G Messer, et al.
Immunogenetics|January 1, 1991
Developmental and tissue-specific expression of the Q5k geneS Schwemmle, D Bevec, G Brem, et al.
American Journal of Medical Genetics|June 27, 1997
XX-agonadism in a fetus with multiple dysraphic lesions: a new syndromeI Kennerknecht, T Mattfeldt, W Paulus, et al.
Genomics|July 1, 1993
Multipoint mapping of the central core disease locusS Schwemmle, K Wolff, L M Palmucci, et al.
American Journal of Human Genetics|June 1, 1997
Characterization of FMR1 promoter elements by in vivo-footprinting analysisS Schwemmle, E de Graaff, H Deissler, et al.
Pageof 1