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Current Opinion in Genetics & Development
|
August 5, 1998
Imprinting in Angelman and Prader-Willi syndromes
Y Jiang, T F Tsai, J Bressler, et al.
Nucleic Acids Research
|
February 25, 1989
Additional polymorphism for D7S8 linked to cystic fibrosis including detection by DNA amplification
H Northrup, C Rosenbloom, W E O'Brien, et al.
Clinical Genetics
|
October 1, 1982
Ornithine transcarbamylase deficiency: long-term survival
V V Michels, E Potts, M Walser, et al.
Pediatrics
|
May 1, 1993
Arginase deficiency presenting as cerebral palsy
A E Scheuerle, R McVie, A L Beaudet, et al.
Genomics
|
March 20, 1995
Cloning and mapping of the mouse alpha 7-neuronal nicotinic acetylcholine receptor
A Orr-Urtreger, M F Seldin, A Baldini, et al.
Lancet (London, England)
|
February 15, 2011
Identification of incestuous parental relationships by SNP-based DNA microarrays
C P Schaaf, D A Scott, J Wiszniewska, et al.
The Journal of Thoracic and Cardiovascular Surgery
|
November 1, 1972
Disseminated intravascular coagulation following extracorporeal circulation
A D Boyd, R M Engelman, R L Beaudet, et al.
Lancet (London, England)
|
July 9, 1988
Prenatal diagnosis of cystic fibrosis by DNA amplification for detection of KM-19 polymorphism
G L Feldman, R Williamson, A L Beaudet, et al.
Genesis (New York, N.Y. : 2000)
|
December 11, 2003
Disruption of the genomic imprint in trans with homologous recombination at Snrpn in ES cells
Ting-Fen Tsai, Jan Bressler, Yong-Hui Jiang, et al.
Blood
|
January 5, 2002
Control of leukocyte rolling velocity in TNF-alpha-induced inflammation by LFA-1 and Mac-1
Jessica L Dunne, Christie M Ballantyne, Arthur L Beaudet, et al.
Page
of 46
Search research articles
Search
Showing results (121-130 of 456) with videos related to
Sort By:
Page
of 46
Current Opinion in Genetics & Development
|
August 5, 1998
Imprinting in Angelman and Prader-Willi syndromes
Y Jiang, T F Tsai, J Bressler, et al.
Nucleic Acids Research
|
February 25, 1989
Additional polymorphism for D7S8 linked to cystic fibrosis including detection by DNA amplification
H Northrup, C Rosenbloom, W E O'Brien, et al.
Clinical Genetics
|
October 1, 1982
Ornithine transcarbamylase deficiency: long-term survival
V V Michels, E Potts, M Walser, et al.
Pediatrics
|
May 1, 1993
Arginase deficiency presenting as cerebral palsy
A E Scheuerle, R McVie, A L Beaudet, et al.
Genomics
|
March 20, 1995
Cloning and mapping of the mouse alpha 7-neuronal nicotinic acetylcholine receptor
A Orr-Urtreger, M F Seldin, A Baldini, et al.
Lancet (London, England)
|
February 15, 2011
Identification of incestuous parental relationships by SNP-based DNA microarrays
C P Schaaf, D A Scott, J Wiszniewska, et al.
The Journal of Thoracic and Cardiovascular Surgery
|
November 1, 1972
Disseminated intravascular coagulation following extracorporeal circulation
A D Boyd, R M Engelman, R L Beaudet, et al.
Lancet (London, England)
|
July 9, 1988
Prenatal diagnosis of cystic fibrosis by DNA amplification for detection of KM-19 polymorphism
G L Feldman, R Williamson, A L Beaudet, et al.
Genesis (New York, N.Y. : 2000)
|
December 11, 2003
Disruption of the genomic imprint in trans with homologous recombination at Snrpn in ES cells
Ting-Fen Tsai, Jan Bressler, Yong-Hui Jiang, et al.
Blood
|
January 5, 2002
Control of leukocyte rolling velocity in TNF-alpha-induced inflammation by LFA-1 and Mac-1
Jessica L Dunne, Christie M Ballantyne, Arthur L Beaudet, et al.
Page
of 46