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J A Lamb

Showing results (11-20 of 16) with videos related to

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Molecular Psychiatry|November 1, 2003
Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII geneE Bacchelli, F Blasi, M Biondolillo, et al.
Arthritis and Rheumatism|September 30, 2008
The protein tyrosine phosphatase N22 gene is associated with juvenile and adult idiopathic inflammatory myopathy independent of the HLA 8.1 haplotype in British Caucasian patientsH Chinoy, H Platt, J A Lamb, et al.
American Journal of Human Genetics|March 15, 2002
FOXP2 is not a major susceptibility gene for autism or specific language impairmentD F Newbury, E Bonora, J A Lamb, et al.
Molecular Psychiatry|April 30, 2009
High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibilityE Maestrini, A T Pagnamenta, J A Lamb, et al.
Genes and Immunity|August 21, 2015
Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypesF W Miller, W Chen, T P O'Hanlon, et al.
Annals of the Rheumatic Diseases|January 27, 2017
Cytosolic 5'-nucleotidase 1A autoantibody profile and clinical characteristics in inclusion body myositisJ B Lilleker, A Rietveld, S R Pye, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Molecular Psychiatry|November 1, 2003
Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII geneE Bacchelli, F Blasi, M Biondolillo, et al.
Arthritis and Rheumatism|September 30, 2008
The protein tyrosine phosphatase N22 gene is associated with juvenile and adult idiopathic inflammatory myopathy independent of the HLA 8.1 haplotype in British Caucasian patientsH Chinoy, H Platt, J A Lamb, et al.
American Journal of Human Genetics|March 15, 2002
FOXP2 is not a major susceptibility gene for autism or specific language impairmentD F Newbury, E Bonora, J A Lamb, et al.
Molecular Psychiatry|April 30, 2009
High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibilityE Maestrini, A T Pagnamenta, J A Lamb, et al.
Genes and Immunity|August 21, 2015
Genome-wide association study identifies HLA 8.1 ancestral haplotype alleles as major genetic risk factors for myositis phenotypesF W Miller, W Chen, T P O'Hanlon, et al.
Annals of the Rheumatic Diseases|January 27, 2017
Cytosolic 5'-nucleotidase 1A autoantibody profile and clinical characteristics in inclusion body myositisJ B Lilleker, A Rietveld, S R Pye, et al.
Pageof 2