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Proceedings of the National Academy of Sciences of the United States of America
|
June 1, 1985
Differential amplification, assembly, and relocation of multiple DNA sequences in human neuroblastomas and neuroblastoma cell lines
Y Shiloh, J Shipley, G M Brodeur, et al.
Genomics
|
July 1, 1988
Human monoamine oxidase gene (MAOA): chromosome position (Xp21-p11) and DNA polymorphism
L Ozelius, Y P Hsu, G Bruns, et al.
Genomics
|
August 1, 1988
The poliovirus sensitivity (PVS) gene is on chromosome 19q12----q13.2
T Siddique, R McKinney, W Y Hung, et al.
Veterinary Journal (London, England : 1997)
|
July 13, 2012
Porcine ear necrosis syndrome: a preliminary investigation of putative infectious agents in piglets and mycotoxins in feed
C Weissenbacher-Lang, T Voglmayr, F Waxenecker, et al.
Science (New York, N.Y.)
|
March 27, 1987
A new probe for the diagnosis of myotonic muscular dystrophy
R J Bartlett, M A Pericak-Vance, L Yamaoka, et al.
Genomics
|
July 1, 1988
Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers
S P Kwan, L A Sandkuyl, M Blaese, et al.
American Journal of Human Genetics
|
March 1, 1985
Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus
B de Martinville, L M Kunkel, G Bruns, et al.
Human Molecular Genetics
|
May 1, 1992
The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3
K B Sims, R V Lebo, G Benson, et al.
Journal of Neurogenetics
|
December 1, 1985
Localization of cloned unique DNA to three different regions of chromosome 19: screen for linkage probes for myotonic dystrophy
L H Yamaoka, R J Bartlett, D A Ross, et al.
Neuron
|
January 1, 1989
Monoamine oxidase deficiency in males with an X chromosome deletion
K B Sims, A de la Chapelle, R Norio, et al.
Page
of 7
Search research articles
Search
Showing results (51-60 of 62) with videos related to
Sort By:
Page
of 7
Proceedings of the National Academy of Sciences of the United States of America
|
June 1, 1985
Differential amplification, assembly, and relocation of multiple DNA sequences in human neuroblastomas and neuroblastoma cell lines
Y Shiloh, J Shipley, G M Brodeur, et al.
Genomics
|
July 1, 1988
Human monoamine oxidase gene (MAOA): chromosome position (Xp21-p11) and DNA polymorphism
L Ozelius, Y P Hsu, G Bruns, et al.
Genomics
|
August 1, 1988
The poliovirus sensitivity (PVS) gene is on chromosome 19q12----q13.2
T Siddique, R McKinney, W Y Hung, et al.
Veterinary Journal (London, England : 1997)
|
July 13, 2012
Porcine ear necrosis syndrome: a preliminary investigation of putative infectious agents in piglets and mycotoxins in feed
C Weissenbacher-Lang, T Voglmayr, F Waxenecker, et al.
Science (New York, N.Y.)
|
March 27, 1987
A new probe for the diagnosis of myotonic muscular dystrophy
R J Bartlett, M A Pericak-Vance, L Yamaoka, et al.
Genomics
|
July 1, 1988
Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers
S P Kwan, L A Sandkuyl, M Blaese, et al.
American Journal of Human Genetics
|
March 1, 1985
Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus
B de Martinville, L M Kunkel, G Bruns, et al.
Human Molecular Genetics
|
May 1, 1992
The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3
K B Sims, R V Lebo, G Benson, et al.
Journal of Neurogenetics
|
December 1, 1985
Localization of cloned unique DNA to three different regions of chromosome 19: screen for linkage probes for myotonic dystrophy
L H Yamaoka, R J Bartlett, D A Ross, et al.
Neuron
|
January 1, 1989
Monoamine oxidase deficiency in males with an X chromosome deletion
K B Sims, A de la Chapelle, R Norio, et al.
Page
of 7