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Nature Genetics
|
April 1, 1992
Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A
J R Lupski, C A Wise, A Kuwano, et al.
The Journal of Biological Chemistry
|
January 25, 1988
Human hepatic lipase. Cloned cDNA sequence, restriction fragment length polymorphisms, chromosomal localization, and evolutionary relationships with lipoprotein lipase and pancreatic lipase
S Datta, C C Luo, W H Li, et al.
American Journal of Medical Genetics
|
September 15, 1994
A variety of genetic mechanisms are associated with the Prader-Willi syndrome
T Woodage, Z M Deng, M Prasad, et al.
Science (New York, N.Y.)
|
June 2, 1989
Two NF1 translocations map within a 600-kilobase segment of 17q11.2
P O'Connell, R Leach, R M Cawthon, et al.
Genomics
|
September 1, 1992
The CCAAT/enhancer binding protein (C/EBP alpha) gene (CEBPA) maps to human chromosome 19q13.1 and the related nuclear factor NF-IL6 (C/EBP beta) gene (CEBPB) maps to human chromosome 20q13.1
L R Hendricks-Taylor, L L Bachinski, M J Siciliano, et al.
Somatic Cell and Molecular Genetics
|
July 1, 1987
Human interstitial retinol-binding protein (IRBP): cloning, partial sequence, and chromosomal localization
G I Liou, S L Fong, J Gosden, et al.
American Journal of Obstetrics and Gynecology
|
February 1, 1990
Cytogenetic results of chorionic villus sampling: high success rate and diagnostic accuracy in the United States collaborative study
D H Ledbetter, A O Martin, Y Verlinsky, et al.
American Journal of Human Genetics
|
November 1, 1992
Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM
R A Bascom, J García-Heras, C L Hsieh, et al.
Genomics
|
December 1, 1993
A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN gene
A Mutirangura, A Jayakumar, J S Sutcliffe, et al.
Nature Genetics
|
August 11, 1998
Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality
S Hirotsune, M W Fleck, M J Gambello, et al.
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Search research articles
Search
Showing results (191-200 of 251) with videos related to
Sort By:
Page
of 26
Nature Genetics
|
April 1, 1992
Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A
J R Lupski, C A Wise, A Kuwano, et al.
The Journal of Biological Chemistry
|
January 25, 1988
Human hepatic lipase. Cloned cDNA sequence, restriction fragment length polymorphisms, chromosomal localization, and evolutionary relationships with lipoprotein lipase and pancreatic lipase
S Datta, C C Luo, W H Li, et al.
American Journal of Medical Genetics
|
September 15, 1994
A variety of genetic mechanisms are associated with the Prader-Willi syndrome
T Woodage, Z M Deng, M Prasad, et al.
Science (New York, N.Y.)
|
June 2, 1989
Two NF1 translocations map within a 600-kilobase segment of 17q11.2
P O'Connell, R Leach, R M Cawthon, et al.
Genomics
|
September 1, 1992
The CCAAT/enhancer binding protein (C/EBP alpha) gene (CEBPA) maps to human chromosome 19q13.1 and the related nuclear factor NF-IL6 (C/EBP beta) gene (CEBPB) maps to human chromosome 20q13.1
L R Hendricks-Taylor, L L Bachinski, M J Siciliano, et al.
Somatic Cell and Molecular Genetics
|
July 1, 1987
Human interstitial retinol-binding protein (IRBP): cloning, partial sequence, and chromosomal localization
G I Liou, S L Fong, J Gosden, et al.
American Journal of Obstetrics and Gynecology
|
February 1, 1990
Cytogenetic results of chorionic villus sampling: high success rate and diagnostic accuracy in the United States collaborative study
D H Ledbetter, A O Martin, Y Verlinsky, et al.
American Journal of Human Genetics
|
November 1, 1992
Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGM
R A Bascom, J García-Heras, C L Hsieh, et al.
Genomics
|
December 1, 1993
A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11-q13) and refined localization of the SNRPN gene
A Mutirangura, A Jayakumar, J S Sutcliffe, et al.
Nature Genetics
|
August 11, 1998
Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality
S Hirotsune, M W Fleck, M J Gambello, et al.
Page
of 26