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Journal of Medical Genetics
|
January 11, 2000
Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome
J R Engel, A Smallwood, A Harper, et al.
Molecular and Cellular Biology
|
May 11, 2000
Telomere maintenance in telomerase-deficient mouse embryonic stem cells: characterization of an amplified telomeric DNA
H Niida, Y Shinkai, M P Hande, et al.
Human Molecular Genetics
|
February 7, 2001
Large-scale evaluation of imprinting status in the Prader-Willi syndrome region: an imprinted direct repeat cluster resembling small nucleolar RNA genes
M Meguro, K Mitsuya, N Nomura, et al.
Cancer Genetics and Cytogenetics
|
May 1, 1983
A summary of cytogenetic studies on 534 cases of chronic myelocytic leukemia in Japan
T Ishihara, M Sasaki, M Oshimura, et al.
Genomics
|
November 20, 1995
Isolation and mapping of human homologues of an imprinted mouse gene U2af1-rs1
K Kitagawa, X Wang, I Hatada, et al.
Genomics
|
July 20, 1995
Construction of 110 cosmid markers and a 4.5-Mb YAC contig on human chromosome 8p12-q11
A Kurimasa, N Suzuki, S Kumano, et al.
Genomics
|
August 1, 1992
Assignment of a human DNA double-strand break repair gene (XRCC5) to chromosome 2
D J Chen, M S Park, E Campbell, et al.
Oncogene
|
July 1, 1993
Deletion mapping of chromosome 3p in human uterine cervical cancer
T Kohno, H Takayama, M Hamaguchi, et al.
Biochimica Et Biophysica Acta
|
January 6, 1992
Structure of the human pituitary adenylate cyclase activating polypeptide (PACAP) gene
M Hosoya, C Kimura, K Ogi, et al.
Human Molecular Genetics
|
July 13, 2001
A conserved imprinting control region at the HYMAI/ZAC domain is implicated in transient neonatal diabetes mellitus
T Arima, R A Drewell, K L Arney, et al.
Page
of 25
Search research articles
Search
Showing results (201-210 of 242) with videos related to
Sort By:
Page
of 25
Journal of Medical Genetics
|
January 11, 2000
Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome
J R Engel, A Smallwood, A Harper, et al.
Molecular and Cellular Biology
|
May 11, 2000
Telomere maintenance in telomerase-deficient mouse embryonic stem cells: characterization of an amplified telomeric DNA
H Niida, Y Shinkai, M P Hande, et al.
Human Molecular Genetics
|
February 7, 2001
Large-scale evaluation of imprinting status in the Prader-Willi syndrome region: an imprinted direct repeat cluster resembling small nucleolar RNA genes
M Meguro, K Mitsuya, N Nomura, et al.
Cancer Genetics and Cytogenetics
|
May 1, 1983
A summary of cytogenetic studies on 534 cases of chronic myelocytic leukemia in Japan
T Ishihara, M Sasaki, M Oshimura, et al.
Genomics
|
November 20, 1995
Isolation and mapping of human homologues of an imprinted mouse gene U2af1-rs1
K Kitagawa, X Wang, I Hatada, et al.
Genomics
|
July 20, 1995
Construction of 110 cosmid markers and a 4.5-Mb YAC contig on human chromosome 8p12-q11
A Kurimasa, N Suzuki, S Kumano, et al.
Genomics
|
August 1, 1992
Assignment of a human DNA double-strand break repair gene (XRCC5) to chromosome 2
D J Chen, M S Park, E Campbell, et al.
Oncogene
|
July 1, 1993
Deletion mapping of chromosome 3p in human uterine cervical cancer
T Kohno, H Takayama, M Hamaguchi, et al.
Biochimica Et Biophysica Acta
|
January 6, 1992
Structure of the human pituitary adenylate cyclase activating polypeptide (PACAP) gene
M Hosoya, C Kimura, K Ogi, et al.
Human Molecular Genetics
|
July 13, 2001
A conserved imprinting control region at the HYMAI/ZAC domain is implicated in transient neonatal diabetes mellitus
T Arima, R A Drewell, K L Arney, et al.
Page
of 25