F Collins

Use of short sequence repeat DNA polymorphisms after PCR amplification to detect the parental origin of the additional chromosome 21 in Down syndrome

Michael B. Petersen, Albert Schinzel, Franz Binkert et al. · PubMed · 1991 · 89 citations · Full text

Clinical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (<i>MAOA</i> and <i>MAOB</i>) genes

F Collins, Dennis L. Murphy, Allan L. Reiss et al. · American Journal of Medical Genetics · 1992 · 75 citations

Marfan syndrome: no evidence for heterogeneity in different populations, and more precise mapping of the gene.

Katariina Kainulainen, B Steinmann, F Collins et al. · PubMed · 1991 · 52 citations