Search research articles
Contact Us
Filters
Showing results (51-60 of 83) with videos related to
Page
of 9
Sort By:
Genomics
|
August 1, 1994
Isolation of a yeast artificial chromosome contig spanning the Greig cephalopolysyndactyly syndrome (GCPS) gene region
A Vortkamp, M Gessler, D Le Paslier, et al.
Human Molecular Genetics
|
May 16, 1998
Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms
B Klamt, A Koziell, F Poulat, et al.
Genes, Chromosomes & Cancer
|
July 1, 1993
Homozygous inactivation of WT1 in a Wilms' tumor associated with the WAGR syndrome
M Gessler, A König, J Moore, et al.
Der Urologe. Ausg. A
|
May 15, 2014
[Adjustable transobturatoric sling system in men : diagnosis and therapy recommendations to persistent pain]
R M Bauer, W Hübner, H-J Knopf, et al.
Human Molecular Genetics
|
September 1, 1992
Human CC10, the homologue of rabbit uteroglobin: genomic cloning, chromosomal localization and expression in endometrial cell lines
M Wolf, J Klug, R Hackenberg, et al.
Nature
|
February 22, 1990
Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping
M Gessler, A Poustka, W Cavenee, et al.
Genomics
|
August 7, 1998
Transcript map of a 900-kb genomic region in Xp22.1-p22.2: identification of 12 novel genes
R Warneke-Wittstock, A Marquardt, A Gehrig, et al.
Human Genetics
|
February 1, 1994
Confirmation of the localization of the human recombination activating gene 1 (RAG1) to chromosome 11p13
K Schwarz, H Hameister, M Gessler, et al.
Human Genetics
|
June 1, 1996
Six new polymorphic microsatellite markers used for the integration of genetic and physical maps of human chromosome 7
S Beck, F Badbanchi, M Otto, et al.
International Journal of Cancer
|
November 16, 2005
Expression profiling of Wilms tumors reveals new candidate genes for different clinical parameters
B Zirn, O Hartmann, B Samans, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 83) with videos related to
Sort By:
Page
of 9
Genomics
|
August 1, 1994
Isolation of a yeast artificial chromosome contig spanning the Greig cephalopolysyndactyly syndrome (GCPS) gene region
A Vortkamp, M Gessler, D Le Paslier, et al.
Human Molecular Genetics
|
May 16, 1998
Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms
B Klamt, A Koziell, F Poulat, et al.
Genes, Chromosomes & Cancer
|
July 1, 1993
Homozygous inactivation of WT1 in a Wilms' tumor associated with the WAGR syndrome
M Gessler, A König, J Moore, et al.
Der Urologe. Ausg. A
|
May 15, 2014
[Adjustable transobturatoric sling system in men : diagnosis and therapy recommendations to persistent pain]
R M Bauer, W Hübner, H-J Knopf, et al.
Human Molecular Genetics
|
September 1, 1992
Human CC10, the homologue of rabbit uteroglobin: genomic cloning, chromosomal localization and expression in endometrial cell lines
M Wolf, J Klug, R Hackenberg, et al.
Nature
|
February 22, 1990
Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping
M Gessler, A Poustka, W Cavenee, et al.
Genomics
|
August 7, 1998
Transcript map of a 900-kb genomic region in Xp22.1-p22.2: identification of 12 novel genes
R Warneke-Wittstock, A Marquardt, A Gehrig, et al.
Human Genetics
|
February 1, 1994
Confirmation of the localization of the human recombination activating gene 1 (RAG1) to chromosome 11p13
K Schwarz, H Hameister, M Gessler, et al.
Human Genetics
|
June 1, 1996
Six new polymorphic microsatellite markers used for the integration of genetic and physical maps of human chromosome 7
S Beck, F Badbanchi, M Otto, et al.
International Journal of Cancer
|
November 16, 2005
Expression profiling of Wilms tumors reveals new candidate genes for different clinical parameters
B Zirn, O Hartmann, B Samans, et al.
Page
of 9