K. Bartlett

Clear Correlation of Genotype with Disease Phenotype in Very–Long-Chain Acyl-CoA Dehydrogenase Deficiency

Brage Storstein Andresen, S. E. Olpin, Ben J. H. M. Poorthuis et al. · The American Journal of Human Genetics · 1999 · 300 citations · Full text

Genetic Diseases, Disease Phenotype, Genetic Determinant +10

Smith-Lemli-Opitz syndrome: a variable clinical and biochemical phenotype.

A K Ryan, K. Bartlett, Peter T. Clayton et al. · Journal of Medical Genetics · 1998 · 234 citations · Full text

Clinical Disorders, Smith-lemli-opitz Syndrome, Mendelian Disorder +9

Short-Chain Acyl-CoA Dehydrogenase Deficiency Associated with a Lipid-Storage Myopathy and Secondary Carnitine Deficiency

Douglass M. Turnbull, K. Bartlett, David L. Stevens et al. · New England Journal of Medicine · 1984 · 135 citations

Electrolyte Disorder, Metabolic Disorder, Endocrine Disease +24

Combined enzyme defect of mitochondrial fatty acid oxidation.

Sandra L. Jackson, Rajinder Singh Kler, K. Bartlett et al. · Journal of Clinical Investigation · 1992 · 128 citations · Full text

Recurrent Episodes, Energy Metabolism, Enzyme Defect +11

The Factorial Survey: An Approach to Defining Sexual Harassment on Campus

Timothy M. Reilly, Sandra Carpenter, Valerie Dul et al. · Journal of Social Issues · 1982 · 114 citations

Gender Identity, Defining Sexual Harassment, Sexual Abuse +11