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L L Field

Showing results (51-60 of 59) with videos related to

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Genes, Brain, and Behavior|March 12, 2014
Association of the ROBO1 gene with reading disabilities in a family-based analysisC Tran, K G Wigg, K Zhang, et al.
Journal of Medical Genetics|August 1, 1982
Linkage analysis of five pedigrees affected with typical autosomal dominant retinitis pigmentosaL L Field, J R Heckenlively, R S Sparkes, et al.
American Journal of Human Genetics|November 1, 1983
The Tay-Sachs disease gene in North American Jewish populations: geographic variations and originG M Petersen, J I Rotter, R M Cantor, et al.
Human Heredity|January 1, 1984
Estimating the recombination frequency for the MN and the Ss lociM A Spence, L L Field, M L Marazita, et al.
Human Genetics|January 1, 1984
Estimating the recombination frequency for the PTC-Kell linkageM Anne-Spence, C T Falk, K Neiswanger, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 24, 2013
A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1C Tran, F Gagnon, K G Wigg, et al.
Lancet (London, England)|October 24, 1981
Close genetic linkage between diabetes mellitus and kidd blood groupS E Hodge, C E Anderson, K Neiswanger, et al.
Nature Genetics|September 14, 2004
A specific requirement for PDGF-C in palate formation and PDGFR-alpha signalingHao Ding, Xiaoli Wu, Hans Boström, et al.
Journal of Dental Research|February 29, 2012
Association of AXIN2 with non-syndromic oral clefts in multiple populationsA Letra, B Bjork, M E Cooper, et al.
Pageof 6

Showing results (51-60 of 59) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 59 results.
Genes, Brain, and Behavior|March 12, 2014
Association of the ROBO1 gene with reading disabilities in a family-based analysisC Tran, K G Wigg, K Zhang, et al.
Journal of Medical Genetics|August 1, 1982
Linkage analysis of five pedigrees affected with typical autosomal dominant retinitis pigmentosaL L Field, J R Heckenlively, R S Sparkes, et al.
American Journal of Human Genetics|November 1, 1983
The Tay-Sachs disease gene in North American Jewish populations: geographic variations and originG M Petersen, J I Rotter, R M Cantor, et al.
Human Heredity|January 1, 1984
Estimating the recombination frequency for the MN and the Ss lociM A Spence, L L Field, M L Marazita, et al.
Human Genetics|January 1, 1984
Estimating the recombination frequency for the PTC-Kell linkageM Anne-Spence, C T Falk, K Neiswanger, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 24, 2013
A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1C Tran, F Gagnon, K G Wigg, et al.
Lancet (London, England)|October 24, 1981
Close genetic linkage between diabetes mellitus and kidd blood groupS E Hodge, C E Anderson, K Neiswanger, et al.
Nature Genetics|September 14, 2004
A specific requirement for PDGF-C in palate formation and PDGFR-alpha signalingHao Ding, Xiaoli Wu, Hans Boström, et al.
Journal of Dental Research|February 29, 2012
Association of AXIN2 with non-syndromic oral clefts in multiple populationsA Letra, B Bjork, M E Cooper, et al.
Pageof 6