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I W Craig

Showing results (111-120 of 132) with videos related to

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Journal of Molecular Biology|April 20, 1985
Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosomeJ Wolfe, S M Darling, R P Erickson, et al.
Genomics|May 1, 1991
Localization of the gene for the Wiskott-Aldrich syndrome between two flanking markers, TIMP and DXS255, on Xp11.22-Xp11.3S P Kwan, T Lehner, T Hagemann, et al.
Genomics|May 1, 1993
Norrie disease gene: characterization of deletions and possible functionZ Y Chen, E M Battinelli, R W Hendriks, et al.
Human Genetics|March 1, 1989
Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on XpA Gal, A Schinzel, U Orth, et al.
Human Molecular Genetics|July 1, 1994
Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemiaK A Rack, J Chelly, R J Gibbons, et al.
Behavior Genetics|February 13, 2002
A genome-wide scan of 1842 DNA markers for allelic associations with general cognitive ability: a five-stage design using DNA pooling and extreme selected groupsR Plomin, L Hill, I W Craig, et al.
Human Molecular Genetics|May 1, 1992
The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3K B Sims, R V Lebo, G Benson, et al.
Genomics|April 1, 1994
A 2-Mb YAC contig encompassing three loci (DXF34, DXS14, and DXS390) that lie between Xp11.2 translocation breakpoints associated with incontinentia pigmenti type 1V Reed, S Rider, G L Maslen, et al.
Nature|January 3, 1991
Localization of the X inactivation centre on the human X chromosome in Xq13C J Brown, R G Lafreniere, V E Powers, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 16, 2009
NRG1 gene in recurrent major depression: no association in a large-scale case-control association studyA Schosser, S Cohen-Woods, D Gaysina, et al.
Pageof 14

Showing results (111-120 of 132) with videos related to

Sort By:
Pageof 14
Journal of Molecular Biology|April 20, 1985
Isolation and characterization of an alphoid centromeric repeat family from the human Y chromosomeJ Wolfe, S M Darling, R P Erickson, et al.
Genomics|May 1, 1991
Localization of the gene for the Wiskott-Aldrich syndrome between two flanking markers, TIMP and DXS255, on Xp11.22-Xp11.3S P Kwan, T Lehner, T Hagemann, et al.
Genomics|May 1, 1993
Norrie disease gene: characterization of deletions and possible functionZ Y Chen, E M Battinelli, R W Hendriks, et al.
Human Genetics|March 1, 1989
Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on XpA Gal, A Schinzel, U Orth, et al.
Human Molecular Genetics|July 1, 1994
Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemiaK A Rack, J Chelly, R J Gibbons, et al.
Behavior Genetics|February 13, 2002
A genome-wide scan of 1842 DNA markers for allelic associations with general cognitive ability: a five-stage design using DNA pooling and extreme selected groupsR Plomin, L Hill, I W Craig, et al.
Human Molecular Genetics|May 1, 1992
The Norrie disease gene maps to a 150 kb region on chromosome Xp11.3K B Sims, R V Lebo, G Benson, et al.
Genomics|April 1, 1994
A 2-Mb YAC contig encompassing three loci (DXF34, DXS14, and DXS390) that lie between Xp11.2 translocation breakpoints associated with incontinentia pigmenti type 1V Reed, S Rider, G L Maslen, et al.
Nature|January 3, 1991
Localization of the X inactivation centre on the human X chromosome in Xq13C J Brown, R G Lafreniere, V E Powers, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 16, 2009
NRG1 gene in recurrent major depression: no association in a large-scale case-control association studyA Schosser, S Cohen-Woods, D Gaysina, et al.
Pageof 14