R F Wintle - JoVE Visualize

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Genomics|September 1, 1994

Mapping of human immunoglobulin heavy chain variable gene segments outside the major IGH locusR F Wintle, D W Cox

Parkinsonism & Related Disorders|May 2, 2001

Dopamine signaling in Caenorhabditis elegans-potential for parkinsonism researchR F. Wintle, H H.M. Van Tol

Cytogenetics and Cell Genetics|January 1, 1990

In situ hybridization to human chromosome 1 of a cDNA probe for the gene encoding the basement membrane heparan sulfate proteoglycan (HSPG)R F Wintle, R Kisilevsky, D Noonan, et al.

Genomics|March 15, 1997

Genetic polymorphism and recombination in the subtelomeric region of chromosome 14qR F Wintle, T G Nygaard, J A Herbrick, et al.

Human Genetics|May 1, 1995

Molecular analysis redefines three human chromosome 14 deletionsR F Wintle, T Costa, R H Haslam, et al.

Cytogenetic and Genome Research|March 17, 2009

Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reportingS Goobie, J Knijnenburg, D Fitzpatrick, et al.

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

Sort By:

Pageof 1

Genomics|September 1, 1994

Mapping of human immunoglobulin heavy chain variable gene segments outside the major IGH locusR F Wintle, D W Cox

Parkinsonism & Related Disorders|May 2, 2001

Dopamine signaling in Caenorhabditis elegans-potential for parkinsonism researchR F. Wintle, H H.M. Van Tol

Cytogenetics and Cell Genetics|January 1, 1990

In situ hybridization to human chromosome 1 of a cDNA probe for the gene encoding the basement membrane heparan sulfate proteoglycan (HSPG)R F Wintle, R Kisilevsky, D Noonan, et al.

Genomics|March 15, 1997

Genetic polymorphism and recombination in the subtelomeric region of chromosome 14qR F Wintle, T G Nygaard, J A Herbrick, et al.

Human Genetics|May 1, 1995

Molecular analysis redefines three human chromosome 14 deletionsR F Wintle, T Costa, R H Haslam, et al.

Cytogenetic and Genome Research|March 17, 2009

Molecular and clinical characterization of de novo and familial cases with microduplication 3q29: guidelines for copy number variation case reportingS Goobie, J Knijnenburg, D Fitzpatrick, et al.

Pageof 1