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The Journal of Clinical Investigation
|
June 14, 2005
Functional, structural, and metabolic abnormalities of the hippocampal formation in Williams syndrome
Andreas Meyer-Lindenberg, Carolyn B Mervis, Deepak Sarpal, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 11, 2007
Genetic contributions to white matter architecture revealed by diffusion tensor imaging in Williams syndrome
Stefano Marenco, Michael A Siuta, J Shane Kippenhan, et al.
American Journal of Medical Genetics. Part A
|
September 4, 2015
7q11.23 Duplication syndrome: Physical characteristics and natural history
Colleen A Morris, Carolyn B Mervis, Alex P Paciorkowski, et al.
Plos One
|
September 9, 2010
Genome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndrome
Ariel M Pani, Holly H Hobart, Colleen A Morris, et al.
Journal of Neurodevelopmental Disorders
|
August 26, 2023
Dorsal visual stream and LIMK1: hemideletion, haplotype, and enduring effects in children with Williams syndrome
J Shane Kippenhan, Michael D Gregory, Tiffany Nash, et al.
The New England Journal of Medicine
|
October 21, 2005
Severe expressive-language delay related to duplication of the Williams-Beuren locus
Martin J Somerville, Carolyn B Mervis, Edwin J Young, et al.
American Journal of Medical Genetics. Part A
|
October 14, 2003
GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome region
Colleen A Morris, Carolyn B Mervis, Holly H Hobart, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 27, 2008
Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management
Angela E Lin, Craig T Basson, Elizabeth Goldmuntz, et al.
Nature Genetics
|
May 18, 2004
Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B
Ian D Krantz, Jennifer McCallum, Cheryl DeScipio, et al.
American Journal of Human Genetics
|
June 21, 2008
Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11
Christian R Marshall, Edwin J Young, Ariel M Pani, et al.
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of 5
Search research articles
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Showing results (31-40 of 43) with videos related to
Sort By:
Page
of 5
The Journal of Clinical Investigation
|
June 14, 2005
Functional, structural, and metabolic abnormalities of the hippocampal formation in Williams syndrome
Andreas Meyer-Lindenberg, Carolyn B Mervis, Deepak Sarpal, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
September 11, 2007
Genetic contributions to white matter architecture revealed by diffusion tensor imaging in Williams syndrome
Stefano Marenco, Michael A Siuta, J Shane Kippenhan, et al.
American Journal of Medical Genetics. Part A
|
September 4, 2015
7q11.23 Duplication syndrome: Physical characteristics and natural history
Colleen A Morris, Carolyn B Mervis, Alex P Paciorkowski, et al.
Plos One
|
September 9, 2010
Genome rearrangements detected by SNP microarrays in individuals with intellectual disability referred with possible Williams syndrome
Ariel M Pani, Holly H Hobart, Colleen A Morris, et al.
Journal of Neurodevelopmental Disorders
|
August 26, 2023
Dorsal visual stream and LIMK1: hemideletion, haplotype, and enduring effects in children with Williams syndrome
J Shane Kippenhan, Michael D Gregory, Tiffany Nash, et al.
The New England Journal of Medicine
|
October 21, 2005
Severe expressive-language delay related to duplication of the Williams-Beuren locus
Martin J Somerville, Carolyn B Mervis, Edwin J Young, et al.
American Journal of Medical Genetics. Part A
|
October 14, 2003
GTF2I hemizygosity implicated in mental retardation in Williams syndrome: genotype-phenotype analysis of five families with deletions in the Williams syndrome region
Colleen A Morris, Carolyn B Mervis, Holly H Hobart, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 27, 2008
Adults with genetic syndromes and cardiovascular abnormalities: clinical history and management
Angela E Lin, Craig T Basson, Elizabeth Goldmuntz, et al.
Nature Genetics
|
May 18, 2004
Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B
Ian D Krantz, Jennifer McCallum, Cheryl DeScipio, et al.
American Journal of Human Genetics
|
June 21, 2008
Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11
Christian R Marshall, Edwin J Young, Ariel M Pani, et al.
Page
of 5