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International Journal of Cancer
|
May 8, 2000
Genomic structure and mutation screening of the E2F4 gene in human tumors
S 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 repeat
P 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-inactivation
W 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 stability
D 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, Q5k
E H Weiss, D Bevec, G Messer, et al.
Immunogenetics
|
January 1, 1991
Developmental and tissue-specific expression of the Q5k gene
S 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 syndrome
I Kennerknecht, T Mattfeldt, W Paulus, et al.
Genomics
|
July 1, 1993
Multipoint mapping of the central core disease locus
S 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 analysis
S Schwemmle, E de Graaff, H Deissler, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
International Journal of Cancer
|
May 8, 2000
Genomic structure and mutation screening of the E2F4 gene in human tumors
S 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 repeat
P 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-inactivation
W 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 stability
D 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, Q5k
E H Weiss, D Bevec, G Messer, et al.
Immunogenetics
|
January 1, 1991
Developmental and tissue-specific expression of the Q5k gene
S 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 syndrome
I Kennerknecht, T Mattfeldt, W Paulus, et al.
Genomics
|
July 1, 1993
Multipoint mapping of the central core disease locus
S 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 analysis
S Schwemmle, E de Graaff, H Deissler, et al.
Page
of 1