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L R Osborne

Showing results (11-20 of 22) with videos related to

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Gene|February 5, 1999
The BCL7 gene family: deletion of BCL7B in Williams syndromeD M Jadayel, L R Osborne, L J Coignet, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 29, 2010
High prevalence of diabetes and pre-diabetes in adults with Williams syndromeB R Pober, E Wang, S Caprio, et al.
Journal of Medical Genetics|June 30, 2000
Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genesA Botta, G Novelli, A Mari, et al.
Human Molecular Genetics|October 1, 1993
Nasal epithelial ion transport and genetic analysis of infertile men with congenital bilateral absence of the vas deferensL R Osborne, M Lynch, P G Middleton, et al.
Nature Genetics|October 31, 2001
A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndromeL R Osborne, M Li, B Pober, et al.
Genes, Brain, and Behavior|August 8, 2007
Reduced fear and aggression and altered serotonin metabolism in Gtf2ird1-targeted miceE J Young, T Lipina, E Tam, et al.
Genes, Brain, and Behavior|March 23, 2007
Forward genetic screen of mouse reveals dominant missense mutation in the P/Q-type voltage-dependent calcium channel, CACNA1AG Xie, S J Clapcote, B J Nieman, et al.
Genomics|September 1, 1996
Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patientsL R Osborne, D Martindale, S W Scherer, et al.
Medrxiv : the Preprint Server for Health Sciences|October 7, 2024
Identifying individuals at risk for surgical supravalvar aortic stenosis by polygenic risk score with graded phenotypingD Liu, C B Mervis, M D Levin, et al.
Neurology|May 4, 2011
West syndrome associated with 14q12 duplications harboring FOXG1P Striano, R Paravidino, F Sicca, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
Gene|February 5, 1999
The BCL7 gene family: deletion of BCL7B in Williams syndromeD M Jadayel, L R Osborne, L J Coignet, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 29, 2010
High prevalence of diabetes and pre-diabetes in adults with Williams syndromeB R Pober, E Wang, S Caprio, et al.
Journal of Medical Genetics|June 30, 2000
Detection of an atypical 7q11.23 deletion in Williams syndrome patients which does not include the STX1A and FZD3 genesA Botta, G Novelli, A Mari, et al.
Human Molecular Genetics|October 1, 1993
Nasal epithelial ion transport and genetic analysis of infertile men with congenital bilateral absence of the vas deferensL R Osborne, M Lynch, P G Middleton, et al.
Nature Genetics|October 31, 2001
A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndromeL R Osborne, M Li, B Pober, et al.
Genes, Brain, and Behavior|August 8, 2007
Reduced fear and aggression and altered serotonin metabolism in Gtf2ird1-targeted miceE J Young, T Lipina, E Tam, et al.
Genes, Brain, and Behavior|March 23, 2007
Forward genetic screen of mouse reveals dominant missense mutation in the P/Q-type voltage-dependent calcium channel, CACNA1AG Xie, S J Clapcote, B J Nieman, et al.
Genomics|September 1, 1996
Identification of genes from a 500-kb region at 7q11.23 that is commonly deleted in Williams syndrome patientsL R Osborne, D Martindale, S W Scherer, et al.
Medrxiv : the Preprint Server for Health Sciences|October 7, 2024
Identifying individuals at risk for surgical supravalvar aortic stenosis by polygenic risk score with graded phenotypingD Liu, C B Mervis, M D Levin, et al.
Neurology|May 4, 2011
West syndrome associated with 14q12 duplications harboring FOXG1P Striano, R Paravidino, F Sicca, et al.
Pageof 3