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Human Genetics
|
September 1, 1991
Methods for analysis of multiple cystic fibrosis mutations
I S Ng, R Pace, M V Richard, et al.
Annals of Neurology
|
September 1, 1986
Atypical presentation and neuropathological studies in 3-hydroxy-3-methylglutaryl-CoA lyase deficiency
H Y Zoghbi, J E Spence, A L Beaudet, et al.
The Journal of Experimental Medicine
|
March 17, 1997
The association between alpha4-integrin, P-selectin, and E-selectin in an allergic model of inflammation
S Kanwar, D C Bullard, M J Hickey, et al.
Human Genetics
|
January 1, 1985
A study of restriction fragment length polymorphisms at the human alpha-1-antitrypsin locus
K J Matteson, H Ostrer, A Chakravarti, et al.
The Journal of Biological Chemistry
|
August 17, 2001
Immotile sperm and infertility in mice lacking mitochondrial voltage-dependent anion channel type 3
M J Sampson, W K Decker, A L Beaudet, et al.
American Journal of Human Genetics
|
September 1, 1984
Human chromosomal assignments for 14 argininosuccinate synthetase pseudogenes: cloned DNAs as reagents for cytogenetic analysis
T S Su, R L Nussbaum, S Airhart, et al.
Nature Genetics
|
June 30, 2001
The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice
J Bressler, T F Tsai, M Y Wu, et al.
American Journal of Medical Genetics
|
May 1, 1986
The Perlman familial nephroblastomatosis syndrome
F Greenberg, F Stein, M V Gresik, et al.
Journal of Medical Genetics
|
February 6, 2004
Comparative genomic hybridisation using a proximal 17p BAC/PAC array detects rearrangements responsible for four genomic disorders
C J Shaw, C A Shaw, W Yu, et al.
American Journal of Medical Genetics. Part A
|
September 12, 2012
Duplication of OCRL and adjacent genes associated with autism but not Lowe syndrome
Richard J Schroer, Arthur L Beaudet, Marwan Shinawi, et al.
Page
of 46
Search research articles
Search
Showing results (261-270 of 456) with videos related to
Sort By:
Page
of 46
Human Genetics
|
September 1, 1991
Methods for analysis of multiple cystic fibrosis mutations
I S Ng, R Pace, M V Richard, et al.
Annals of Neurology
|
September 1, 1986
Atypical presentation and neuropathological studies in 3-hydroxy-3-methylglutaryl-CoA lyase deficiency
H Y Zoghbi, J E Spence, A L Beaudet, et al.
The Journal of Experimental Medicine
|
March 17, 1997
The association between alpha4-integrin, P-selectin, and E-selectin in an allergic model of inflammation
S Kanwar, D C Bullard, M J Hickey, et al.
Human Genetics
|
January 1, 1985
A study of restriction fragment length polymorphisms at the human alpha-1-antitrypsin locus
K J Matteson, H Ostrer, A Chakravarti, et al.
The Journal of Biological Chemistry
|
August 17, 2001
Immotile sperm and infertility in mice lacking mitochondrial voltage-dependent anion channel type 3
M J Sampson, W K Decker, A L Beaudet, et al.
American Journal of Human Genetics
|
September 1, 1984
Human chromosomal assignments for 14 argininosuccinate synthetase pseudogenes: cloned DNAs as reagents for cytogenetic analysis
T S Su, R L Nussbaum, S Airhart, et al.
Nature Genetics
|
June 30, 2001
The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice
J Bressler, T F Tsai, M Y Wu, et al.
American Journal of Medical Genetics
|
May 1, 1986
The Perlman familial nephroblastomatosis syndrome
F Greenberg, F Stein, M V Gresik, et al.
Journal of Medical Genetics
|
February 6, 2004
Comparative genomic hybridisation using a proximal 17p BAC/PAC array detects rearrangements responsible for four genomic disorders
C J Shaw, C A Shaw, W Yu, et al.
American Journal of Medical Genetics. Part A
|
September 12, 2012
Duplication of OCRL and adjacent genes associated with autism but not Lowe syndrome
Richard J Schroer, Arthur L Beaudet, Marwan Shinawi, et al.
Page
of 46