Robert W. Marion

Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22

Nandita Quaderi, Susann Schweiger, Karin Gaudenz et al. · Nature Genetics · 1997 · 367 citations

Developmental Anomaly, Opitz G/bbb Syndrome, Developmental Biology +7

Human T-Cell Lymphotropic Virus Type III (HTLV-III) Embryopathy

Robert W. Marion · American journal of diseases of children · 1986 · 164 citations

De Novo Mutations in the Beta-Tubulin Gene TUBB2A Cause Simplified Gyral Patterning and Infantile-Onset Epilepsy

Thomas D. Cushion, Alex R. Paciorkowski, Daniela T. Pilz et al. · The American Journal of Human Genetics · 2014 · 119 citations · Full text

Developmental Biology, Molecular Neuroscience, Genetics +7

Mosaic Epigenetic Dysregulation of Ectodermal Cells in Autism Spectrum Disorder

Esther R. Berko, Masako Suzuki, Faygel Beren et al. · PLoS Genetics · 2014 · 104 citations · Full text

Distinctive Dna Methylation, Brain Development, Epigenetic Change +24

Central nervous system anomalies in Seckel syndrome: Report of a new family and review of the literature

Alan Shanske, Diana Garcia Caride, Lisa Menasse-Palmer et al. · American Journal of Medical Genetics · 1997 · 96 citations · Full text