Robin M. Winter
University of Chicago(US)University College London(GB)
Publications by Year
Research Areas
Craniofacial Disorders and Treatments, Cleft Lip and Palate Research, Congenital Anomalies and Fetal Surgery, Genomic variations and chromosomal abnormalities, Congenital limb and hand anomalies
Most-Cited Works
- → Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome(1995)929 cited
- → Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome(1994)766 cited
- → A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome(1994)622 cited
- → G Protein-Coupled Receptor-Dependent Development of Human Frontal Cortex(2004)521 cited
- → The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation(1995)508 cited
- → Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes(1995)456 cited
- → Subtle chromosomal rearrangements in children with unexplained mental retardation