Carol Booth

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 et al. · The American Journal of Human Genetics · 2005 · 276 citations · Full text

Mendelian Disorder, Genetic Disorder, Medicine +10

A loss of function mutation in the <i>COL9A2</i> gene causes autosomal recessive Stickler syndrome

Stuart G. Baker, Carol Booth, Corrine Fillman et al. · American Journal of Medical Genetics Part A · 2011 · 107 citations

Identification of a case of maternal uniparental disomy of chromosome 10 associated with confined placental mosaicism

C. E. Jones, Carol Booth, Debra Rita et al. · Prenatal Diagnosis · 1995 · 98 citations

A second-site mutation at phenylalanine-137 that increases catalytic efficiency in the mutant aspartate-27 .fwdarw. serine Escherichia coli dihydrofolate reductase

Elizabeth E. Howell, Carol Booth, Martin F. Farnum et al. · Biochemistry · 1990 · 29 citations

Acute myeloid leukemia and myelodysplasia following intensive chemotherapy for breast cancer.

S Roman-Unfer, Bitran Jd, Stephen B. Hanauer et al. · PubMed · 1995 · 29 citations