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American Journal of Human Genetics
|
April 16, 1998
Ataxia with isolated vitamin E deficiency: heterogeneity of mutations and phenotypic variability in a large number of families
L Cavalier, K Ouahchi, H J Kayden, et al.
Human Molecular Genetics
|
October 1, 1994
Identification of a new frameshift mutation (1801delAG) in the ALD gene
A Barceló, M Girós, C O Sarde, et al.
The American Journal on Addictions
|
March 17, 2007
A cognitive behavioral therapy for alcohol-dependent domestic violence offenders: an integrated substance abuse-domestic violence treatment approach (SADV)
Caroline J Easton, Dolores L Mandel, Karen A Hunkele, et al.
Cytogenetics and Cell Genetics
|
January 1, 1989
Report of the committee on the genetic constitution of the X chromosome
J L Mandel, H F Willard, R L Nussbaum, et al.
Journal Francais D'Ophtalmologie
|
March 16, 2005
[Update on Bardet-Biedl syndrome]
H Dollfus, A Verloes, D Bonneau, et al.
Genomics
|
July 1, 1994
Genomic organization of the adrenoleukodystrophy gene
C O Sarde, J Mosser, P Kioschis, et al.
Genomics
|
May 1, 1997
Cloning and characterization of an alternatively spliced gene in proximal Xq28 deleted in two patients with intersexual genitalia and myotubular myopathy
J Laporte, P Kioschis, L J Hu, et al.
Journal of Molecular Biology
|
May 15, 1977
Amanitin binding to RNA polymerase II in alpha-amanitin-resistant rat myoblast mutants
M M Crerar, S J Andrews, E S David, et al.
International Journal of Dermatology
|
February 1, 1993
Classification of skin diseases in nineteenth century America
R J Thomsen, B B Abrams, E H Beutner, et al.
Human Molecular Genetics
|
May 1, 1995
A heterogeneous set of FMR1 proteins is widely distributed in mouse tissues and is modulated in cell culture
E W Khandjian, A Fortin, A Thibodeau, et al.
Page
of 46
Search research articles
Search
Showing results (341-350 of 451) with videos related to
Sort By:
Page
of 46
American Journal of Human Genetics
|
April 16, 1998
Ataxia with isolated vitamin E deficiency: heterogeneity of mutations and phenotypic variability in a large number of families
L Cavalier, K Ouahchi, H J Kayden, et al.
Human Molecular Genetics
|
October 1, 1994
Identification of a new frameshift mutation (1801delAG) in the ALD gene
A Barceló, M Girós, C O Sarde, et al.
The American Journal on Addictions
|
March 17, 2007
A cognitive behavioral therapy for alcohol-dependent domestic violence offenders: an integrated substance abuse-domestic violence treatment approach (SADV)
Caroline J Easton, Dolores L Mandel, Karen A Hunkele, et al.
Cytogenetics and Cell Genetics
|
January 1, 1989
Report of the committee on the genetic constitution of the X chromosome
J L Mandel, H F Willard, R L Nussbaum, et al.
Journal Francais D'Ophtalmologie
|
March 16, 2005
[Update on Bardet-Biedl syndrome]
H Dollfus, A Verloes, D Bonneau, et al.
Genomics
|
July 1, 1994
Genomic organization of the adrenoleukodystrophy gene
C O Sarde, J Mosser, P Kioschis, et al.
Genomics
|
May 1, 1997
Cloning and characterization of an alternatively spliced gene in proximal Xq28 deleted in two patients with intersexual genitalia and myotubular myopathy
J Laporte, P Kioschis, L J Hu, et al.
Journal of Molecular Biology
|
May 15, 1977
Amanitin binding to RNA polymerase II in alpha-amanitin-resistant rat myoblast mutants
M M Crerar, S J Andrews, E S David, et al.
International Journal of Dermatology
|
February 1, 1993
Classification of skin diseases in nineteenth century America
R J Thomsen, B B Abrams, E H Beutner, et al.
Human Molecular Genetics
|
May 1, 1995
A heterogeneous set of FMR1 proteins is widely distributed in mouse tissues and is modulated in cell culture
E W Khandjian, A Fortin, A Thibodeau, et al.
Page
of 46