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P A Wick

Showing results (1-10 of 6) with videos related to

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Human Genetics|May 1, 1995
Intragenic TaqI restriction fragment length polymorphism (RFLP) in CICN4, between the loci for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects syndrome (MLS)R E Schnur, P A Wick
Genomics|March 1, 1993
Deletion mapping and a highly reduced radiation hybrid in the Xp22.3-p22.2 regionR E Schnur, P A Wick, D N Sosnoski, et al.
Journal of Periodontal Research|October 12, 2012
Anti-apolipoprotein A-1 autoantibodies as biomarker for atherosclerosis burden in patients with periodontitisP A Wick, A Mombelli, S Pagano, et al.
The Journal of Investigative Dermatology|May 1, 1996
Type I oculocutaneous albinism associated with a full-length deletion of the tyrosinase geneR E Schnur, B T Sellinger, S A Holmes, et al.
American Journal of Human Genetics|September 1, 1994
Phenotypic variability in X-linked ocular albinism: relationship to linkage genotypesR E Schnur, P A Wick, C Bailey, et al.
American Journal of Human Genetics|June 13, 1998
OA1 mutations and deletions in X-linked ocular albinismR E Schnur, M Gao, P A Wick, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Human Genetics|May 1, 1995
Intragenic TaqI restriction fragment length polymorphism (RFLP) in CICN4, between the loci for X-linked ocular albinism (OA1) and microphthalmia with linear skin defects syndrome (MLS)R E Schnur, P A Wick
Genomics|March 1, 1993
Deletion mapping and a highly reduced radiation hybrid in the Xp22.3-p22.2 regionR E Schnur, P A Wick, D N Sosnoski, et al.
Journal of Periodontal Research|October 12, 2012
Anti-apolipoprotein A-1 autoantibodies as biomarker for atherosclerosis burden in patients with periodontitisP A Wick, A Mombelli, S Pagano, et al.
The Journal of Investigative Dermatology|May 1, 1996
Type I oculocutaneous albinism associated with a full-length deletion of the tyrosinase geneR E Schnur, B T Sellinger, S A Holmes, et al.
American Journal of Human Genetics|September 1, 1994
Phenotypic variability in X-linked ocular albinism: relationship to linkage genotypesR E Schnur, P A Wick, C Bailey, et al.
American Journal of Human Genetics|June 13, 1998
OA1 mutations and deletions in X-linked ocular albinismR E Schnur, M Gao, P A Wick, et al.
Pageof 1