Search research articles
Contact Us
Filters
Showing results (351-360 of 766) with videos related to
Page
of 77
Sort By:
Chromosoma
|
June 1, 1997
Chromosomal evolution of the Chinese muntjac (Muntiacus reevesi)
F Yang, P C O'Brien, J Wienberg, et al.
Obstetrics and Gynecology
|
December 1, 1980
Diagnostic ultrasound: early detection of fetal neural tube defects
H P Robinson, V D Hood, A H Adam, et al.
Mechanisms of Development
|
April 1, 1994
The non-viability of uniparental mouse conceptuses correlates with the loss of the products of imprinted genes
C Walsh, A Glaser, R Fundele, et al.
Human Genetics
|
January 1, 1985
Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophy
D E Wilcox, N A Affara, J R Yates, et al.
Science (New York, N.Y.)
|
March 24, 2012
Trim28 is required for epigenetic stability during mouse oocyte to embryo transition
Daniel M Messerschmidt, Wilhelmine de Vries, Mitsuteru Ito, et al.
Cytogenetics and Cell Genetics
|
December 22, 2000
Dog chromosome-specific paints reveal evolutionary inter- and intrachromosomal rearrangements in the American mink and human
A S Graphodatsky, F Yang, N Serdukova, et al.
Cytogenetics and Cell Genetics
|
January 1, 1978
Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7
E J Winsor, C G Palmer, P M Ellis, et al.
Developmental Cell
|
October 16, 2008
A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints
Xiajun Li, Mitsuteru Ito, Fen Zhou, et al.
Nature
|
June 20, 1991
Embryological and molecular investigations of parental imprinting on mouse chromosome 7
A C Ferguson-Smith, B M Cattanach, S C Barton, et al.
Scottish Medical Journal
|
October 1, 1978
Genotypic and phenotypic family studies of individuals homozygous and heterozygous for HLA-B27, with and without ankylosing spondylitis
D G Spencer, H M Dick, M A Ferguson-Smith, et al.
Page
of 77
Search research articles
Search
Showing results (351-360 of 766) with videos related to
Sort By:
Page
of 77
Chromosoma
|
June 1, 1997
Chromosomal evolution of the Chinese muntjac (Muntiacus reevesi)
F Yang, P C O'Brien, J Wienberg, et al.
Obstetrics and Gynecology
|
December 1, 1980
Diagnostic ultrasound: early detection of fetal neural tube defects
H P Robinson, V D Hood, A H Adam, et al.
Mechanisms of Development
|
April 1, 1994
The non-viability of uniparental mouse conceptuses correlates with the loss of the products of imprinted genes
C Walsh, A Glaser, R Fundele, et al.
Human Genetics
|
January 1, 1985
Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophy
D E Wilcox, N A Affara, J R Yates, et al.
Science (New York, N.Y.)
|
March 24, 2012
Trim28 is required for epigenetic stability during mouse oocyte to embryo transition
Daniel M Messerschmidt, Wilhelmine de Vries, Mitsuteru Ito, et al.
Cytogenetics and Cell Genetics
|
December 22, 2000
Dog chromosome-specific paints reveal evolutionary inter- and intrachromosomal rearrangements in the American mink and human
A S Graphodatsky, F Yang, N Serdukova, et al.
Cytogenetics and Cell Genetics
|
January 1, 1978
Meiotic analysis of a pericentric inversion, inv(7) (p22q32), in the father of a child with a duplication-deletion of chromosome 7
E J Winsor, C G Palmer, P M Ellis, et al.
Developmental Cell
|
October 16, 2008
A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints
Xiajun Li, Mitsuteru Ito, Fen Zhou, et al.
Nature
|
June 20, 1991
Embryological and molecular investigations of parental imprinting on mouse chromosome 7
A C Ferguson-Smith, B M Cattanach, S C Barton, et al.
Scottish Medical Journal
|
October 1, 1978
Genotypic and phenotypic family studies of individuals homozygous and heterozygous for HLA-B27, with and without ankylosing spondylitis
D G Spencer, H M Dick, M A Ferguson-Smith, et al.
Page
of 77