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The Journal of Heart Valve Disease|June 21, 2006
Bilateral semilunar valve disease in a child with partial deletion of the Williams-Beuren syndrome region is associated with elastin haploinsufficiencyRobert B Hinton, Gail H Deutsch, Jeffrey M Pearl, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 29, 2010
Alpha 1 antitrypsin deficiency alleles are associated with joint dislocation and scoliosis in Williams syndromeColleen A Morris, Ariel M Pani, Carolyn B Mervis, et al.
American Journal of Medical Genetics|May 7, 2002
New perspectives on the face in fetal alcohol syndrome: what anthropometry tells usElizabeth S Moore, Richard E Ward, Paul L Jamison, et al.
American Journal of Medical Genetics. Part A|July 3, 2003
Heat shock protein 27 gene: chromosomal and molecular location and relationship to Williams syndromeA Dean Stock, Patricia A Spallone, Thomas R Dennis, et al.
NPJ Genomic Medicine|September 14, 2023
DNA methylation profiles in individuals with rare, atypical 7q11.23 CNVs correlate with GTF2I and GTF2IRD1 copy numberEmma Strong, Carolyn B Mervis, Elaine Tam, et al.
Neuron|September 2, 2004
Neural basis of genetically determined visuospatial construction deficit in Williams syndromeAndreas Meyer-Lindenberg, Philip Kohn, Carolyn B Mervis, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 27, 2005
Genetic contributions to human gyrification: sulcal morphometry in Williams syndromeJ Shane Kippenhan, Rosanna K Olsen, Carolyn B Mervis, et al.
American Journal of Medical Genetics. Part A|February 16, 2018
De novo variants in Myelin regulatory factor (MYRF) as candidates of a new syndrome of cardiac and urogenital anomaliesHailey Pinz, Louise C Pyle, Dong Li, et al.
Developmental Neuropsychology|May 6, 2003
Attentional characteristics of infants and toddlers with Williams syndrome during triadic interactionsCarolyn B Mervis, Colleen A Morris, Bonita P Klein-Tasman, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 14, 2012
The Williams syndrome chromosome 7q11.23 hemideletion confers hypersocial, anxious personality coupled with altered insula structure and functionMbemba Jabbi, J Shane Kippenhan, Philip Kohn, et al.
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