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D Mailman

Showing results (41-50 of 49) with videos related to

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Bioinformatics (Oxford, England)|March 3, 2004
RAD and the RAD Study-Annotator: an approach to collection, organization and exchange of all relevant information for high-throughput gene expression studiesE Manduchi, G R Grant, H He, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 13, 2002
Molecular analysis of spinal muscular atrophy and modification of the phenotype by SMN2Matthew D Mailman, John W Heinz, Audrey C Papp, et al.
Nucleic Acids Research|January 10, 2003
PlasmoDB: the Plasmodium genome resource. A database integrating experimental and computational dataAmit Bahl, Brian Brunk, Jonathan Crabtree, et al.
Nature|October 9, 2002
The Plasmodium genome databaseJessica C Kissinger, Brian P Brunk, Jonathan Crabtree, et al.
Human Genetics|April 3, 2001
Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosomeM D Mailman, T Hemingway, R L Darsey, et al.
Nature Genetics|September 28, 2007
The NCBI dbGaP database of genotypes and phenotypesMatthew D Mailman, Michael Feolo, Yumi Jin, et al.
Plos One|December 7, 2007
Amyotrophic lateral sclerosis: an emerging era of collaborative gene discoveryKatrina Gwinn, Roderick A Corriveau, Hiroshi Mitsumoto, et al.
Nature Genetics|August 31, 2007
New models of collaboration in genome-wide association studies: the Genetic Association Information Network, Teri A Manolio, Laura Lyman Rodriguez, et al.
BMC Medical Genetics|October 2, 2007
The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reportsL Adrienne Cupples, Heather T Arruda, Emelia J Benjamin, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
Bioinformatics (Oxford, England)|March 3, 2004
RAD and the RAD Study-Annotator: an approach to collection, organization and exchange of all relevant information for high-throughput gene expression studiesE Manduchi, G R Grant, H He, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 13, 2002
Molecular analysis of spinal muscular atrophy and modification of the phenotype by SMN2Matthew D Mailman, John W Heinz, Audrey C Papp, et al.
Nucleic Acids Research|January 10, 2003
PlasmoDB: the Plasmodium genome resource. A database integrating experimental and computational dataAmit Bahl, Brian Brunk, Jonathan Crabtree, et al.
Nature|October 9, 2002
The Plasmodium genome databaseJessica C Kissinger, Brian P Brunk, Jonathan Crabtree, et al.
Human Genetics|April 3, 2001
Hybrids monosomal for human chromosome 5 reveal the presence of a spinal muscular atrophy (SMA) carrier with two SMN1 copies on one chromosomeM D Mailman, T Hemingway, R L Darsey, et al.
Nature Genetics|September 28, 2007
The NCBI dbGaP database of genotypes and phenotypesMatthew D Mailman, Michael Feolo, Yumi Jin, et al.
Plos One|December 7, 2007
Amyotrophic lateral sclerosis: an emerging era of collaborative gene discoveryKatrina Gwinn, Roderick A Corriveau, Hiroshi Mitsumoto, et al.
Nature Genetics|August 31, 2007
New models of collaboration in genome-wide association studies: the Genetic Association Information Network, Teri A Manolio, Laura Lyman Rodriguez, et al.
BMC Medical Genetics|October 2, 2007
The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reportsL Adrienne Cupples, Heather T Arruda, Emelia J Benjamin, et al.
Pageof 5