Publications by authors named "Carol Booth"

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A loss of function mutation in the COL9A2 gene causes autosomal recessive Stickler syndrome.
Stuart Baker, Carol Booth, Corrine Fillman, Michael Shapiro, Michael P Blair

Am J Med Genet A· July 2011

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Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals.
Benjamin D Solomon, Felicitas Lacbawan, Sandra Mercier, Nancy J Clegg, Mauricio R Delgado, Carol W Booth

J Med Genet· August 2010

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Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.
Jennifer J Johnston, Isabelle Olivos-Glander, Christina Killoran, Emma Elson, Joyce T Turner, Carol Booth

Am J Hum Genet· April 2005

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Vascular anomalies in Alagille syndrome: a significant cause of morbidity and mortality.
Binita M Kamath, Nancy B Spinner, Karan M Emerick, Albert E Chudley, Carol Booth

Circulation· March 2004

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