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S Kenwrick

Showing results (21-30 of 57) with videos related to

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Nature Genetics|August 1, 1993
A missense mutation confirms the L1 defect in X-linked hydrocephalus (HSAS)M Jouet, A Rosenthal, J MacFarlane, et al.
Cell|January 30, 1987
Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresisS Kenwrick, M Patterson, A Speer, et al.
The Journal of Biological Chemistry|July 4, 2001
Alternative use of a mini exon of the L1 gene affects L1 binding to neural ligandsE De Angelis, T Brummendorf, L Cheng, et al.
American Journal of Medical Genetics|February 5, 1998
Somatic and germ line mosaicism and mutation origin for a mutation in the L1 gene in a family with X-linked hydrocephalusJ S Du, L Bason, H Woffendin, et al.
Molecular and Cellular Neurosciences|May 30, 1998
Alternative splicing of human NrCAM in neural and nonneural tissuesB Wang, H Williams, J S Du, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Molecular analysis of the mature T cell proliferation-1 (MTCP-1) gene in Xq28-linked incontinentia pigmentiH Woffendin, T Esposito, T Jakins, et al.
The EMBO Journal|November 15, 1996
Outline structure of the human L1 cell adhesion molecule and the sites where mutations cause neurological disordersA Bateman, M Jouet, J MacFarlane, et al.
Genomics|July 11, 1992
Sequence of the human factor VIII-associated gene is conserved in mouseB Levinson, J R Bermingham, A Metzenberg, et al.
Nucleic Acids Research|May 11, 1991
A TaqI polymorphism adjacent to the factor VIII gene (F8C)S Kenwrick, P Bridge, D Lillicrap, et al.
Journal of Medical Genetics|March 1, 1993
Refining the genetic location of the gene for X linked hydrocephalus within Xq28M Jouet, E Feldman, J Yates, et al.
Pageof 6

Showing results (21-30 of 57) with videos related to

Sort By:
Pageof 6
Nature Genetics|August 1, 1993
A missense mutation confirms the L1 defect in X-linked hydrocephalus (HSAS)M Jouet, A Rosenthal, J MacFarlane, et al.
Cell|January 30, 1987
Molecular analysis of the Duchenne muscular dystrophy region using pulsed field gel electrophoresisS Kenwrick, M Patterson, A Speer, et al.
The Journal of Biological Chemistry|July 4, 2001
Alternative use of a mini exon of the L1 gene affects L1 binding to neural ligandsE De Angelis, T Brummendorf, L Cheng, et al.
American Journal of Medical Genetics|February 5, 1998
Somatic and germ line mosaicism and mutation origin for a mutation in the L1 gene in a family with X-linked hydrocephalusJ S Du, L Bason, H Woffendin, et al.
Molecular and Cellular Neurosciences|May 30, 1998
Alternative splicing of human NrCAM in neural and nonneural tissuesB Wang, H Williams, J S Du, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Molecular analysis of the mature T cell proliferation-1 (MTCP-1) gene in Xq28-linked incontinentia pigmentiH Woffendin, T Esposito, T Jakins, et al.
The EMBO Journal|November 15, 1996
Outline structure of the human L1 cell adhesion molecule and the sites where mutations cause neurological disordersA Bateman, M Jouet, J MacFarlane, et al.
Genomics|July 11, 1992
Sequence of the human factor VIII-associated gene is conserved in mouseB Levinson, J R Bermingham, A Metzenberg, et al.
Nucleic Acids Research|May 11, 1991
A TaqI polymorphism adjacent to the factor VIII gene (F8C)S Kenwrick, P Bridge, D Lillicrap, et al.
Journal of Medical Genetics|March 1, 1993
Refining the genetic location of the gene for X linked hydrocephalus within Xq28M Jouet, E Feldman, J Yates, et al.
Pageof 6