Peter M. Bingham

The 22q11.2 Deletion: Screening, Diagnostic Workup, and Outcome of Results; Report on 181 Patients

Donna M. McDonald‐McGinn, Don LaRossa, Elizabeth Goldmuntz et al. · Genetic Testing · 1997 · 172 citations

Opitz G/bbb Syndrome, Genetic Epidemiology, Diagnosis +17

Polymicrogyria and deletion 22q11.2 syndrome: Window to the etiology of a common cortical malformation

Nathaniel H. Robin, Clare Taylor, Donna M. McDonald‐McGinn et al. · American Journal of Medical Genetics Part A · 2006 · 147 citations · Full text

Several Brain Malformations, Common Cortical Malformation, Neurological Disorder +18

Stability of an expanded trinucleotide repeat in the androgen receptor gene in transgenic mice

Peter M. Bingham, Marion O. Scott, Suping Wang et al. · Nature Genetics · 1995 · 137 citations

Knockout Mouse, Developmental Biology, Genetics +8

Antecedents of Neonatal Encephalopathy in the Vermont Oxford Network Encephalopathy Registry

Karin B. Nelson, Peter M. Bingham, Erika M. Edwards et al. · PEDIATRICS · 2012 · 113 citations · Full text

Enlarged sylvian fissures in infants with interstitial deletion of chromosome 22q11

Peter M. Bingham, Robert A. Zimmerman, Donna M. McDonald‐McGinn et al. · American Journal of Medical Genetics · 1997 · 93 citations · Full text

Sylvian Fissure Enlargement, Craniofacial Disorder, Cytogenetics +29