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Chromosoma
|
January 1, 1987
Chromosome segregation at meiosis I in female T(2;4)1Gö/+ mice: no evidence for a decreased crossover frequency with maternal age
F Beermann, I Bartels, U Franke, et al.
Cytogenetics and Cell Genetics
|
January 1, 1988
Allocation of a transgenic c-myc integration site to mouse chromosome 8B3-C1
F Beermann, E Hummler, U Franke, et al.
Cytogenetic and Genome Research
|
September 16, 2006
Genomic organization and expression pattern of scapinin (PHACTR3) in mouse and human
S Worch, E Fiedler, I Hansmann, et al.
Human Genetics
|
October 1, 1987
A cytogenetic study directly from chorionic villi of 140 spontaneous abortions
B Eiben, S Borgmann, I Schübbe, et al.
Experimental Cell Research
|
July 1, 1978
Onset of nucleolus organizer activity in early mouse embryogenesis and evidence for its regulation
I Hansmann, J Gebauer, L Bihl, et al.
Human Genetics
|
January 1, 1983
Cytogenic investigation of 103 patients with primary or secondary amenorrhea
O Opitz, B Zoll, I Hansmann, et al.
Journal of Medical Genetics
|
December 1, 1981
A female with XO/XY mosaicism and partial trisomy 9p
M Klasen, I Hansmann, M Schmid, et al.
Human Genetics
|
August 31, 1977
Reciprocal or nonreciprocal human chromosome translocations? The identification of reciprocal translocations by silver staining
I Hansmann, C Wiedeking, T Grimm, et al.
Human Genetics
|
August 1, 1988
Maternal modulation of the inheritable meiosis I error Dipl I in mouse oocytes is associated with the type of mitochondrial DNA
F Beermann, E Hummler, U Franke, et al.
Genomics
|
April 1, 1993
Cystatin C (CST3), the candidate gene for hereditary cystatin C amyloid angiopathy (HCCAA), and other members of the cystatin gene family are clustered on chromosome 20p11.2
S Schnittger, V V Rao, M Abrahamson, et al.
Page
of 13
Search research articles
Search
Showing results (61-70 of 129) with videos related to
Sort By:
Page
of 13
Chromosoma
|
January 1, 1987
Chromosome segregation at meiosis I in female T(2;4)1Gö/+ mice: no evidence for a decreased crossover frequency with maternal age
F Beermann, I Bartels, U Franke, et al.
Cytogenetics and Cell Genetics
|
January 1, 1988
Allocation of a transgenic c-myc integration site to mouse chromosome 8B3-C1
F Beermann, E Hummler, U Franke, et al.
Cytogenetic and Genome Research
|
September 16, 2006
Genomic organization and expression pattern of scapinin (PHACTR3) in mouse and human
S Worch, E Fiedler, I Hansmann, et al.
Human Genetics
|
October 1, 1987
A cytogenetic study directly from chorionic villi of 140 spontaneous abortions
B Eiben, S Borgmann, I Schübbe, et al.
Experimental Cell Research
|
July 1, 1978
Onset of nucleolus organizer activity in early mouse embryogenesis and evidence for its regulation
I Hansmann, J Gebauer, L Bihl, et al.
Human Genetics
|
January 1, 1983
Cytogenic investigation of 103 patients with primary or secondary amenorrhea
O Opitz, B Zoll, I Hansmann, et al.
Journal of Medical Genetics
|
December 1, 1981
A female with XO/XY mosaicism and partial trisomy 9p
M Klasen, I Hansmann, M Schmid, et al.
Human Genetics
|
August 31, 1977
Reciprocal or nonreciprocal human chromosome translocations? The identification of reciprocal translocations by silver staining
I Hansmann, C Wiedeking, T Grimm, et al.
Human Genetics
|
August 1, 1988
Maternal modulation of the inheritable meiosis I error Dipl I in mouse oocytes is associated with the type of mitochondrial DNA
F Beermann, E Hummler, U Franke, et al.
Genomics
|
April 1, 1993
Cystatin C (CST3), the candidate gene for hereditary cystatin C amyloid angiopathy (HCCAA), and other members of the cystatin gene family are clustered on chromosome 20p11.2
S Schnittger, V V Rao, M Abrahamson, et al.
Page
of 13