B. Moghaddam

Natural history of achondroplasia: A retrospective review of longitudinal clinical data

A. Avins, Ericka Okenfuss, B. Moghaddam, 2020, American journal of medical genetics. Part A.

Recurrent HERV‐H‐Mediated 3q13.2–q13.31 Deletions Cause a Syndrome of Hypotonia and Motor, Language, and Cognitive Delays

J. Rosenfeld, L. Shaffer, P. Stankiewicz, 2013, Human mutation.

Minor physical anomalies in children with autism spectrum disorders

I. Hertz-Picciotto, R. Hansen, P. Krakowiak, 2011, Autism : the international journal of research and practice.

Microdeletion 15q13.3: a locus with incomplete penetrance for autism, mental retardation, and psychiatric disorders

P. Stankiewicz, Ankita Patel, J. Lupski, 2009, Journal of Medical Genetics.

Monosomy 21q22.11‐q22.13 presenting as a Fanconi anemia phenotype

M. Steinfeld, R. Byrd, T. Zwerdling, 2011, American journal of medical genetics. Part A.

Molecular and clinical analyses of Greig cephalopolysyndactyly and Pallister-Hall syndromes: robust phenotype prediction from the type and position of GLI3 mutations.

E. Zackai, A. Guttmacher, M. Bamshad, 2005, American journal of human genetics.

Floating–Harbor syndrome and intramedullary spinal cord ganglioglioma: Case report and observations from the literature

W. Ellis, T. Zwerdling, R. Stein-Wexler, 2009, American journal of medical genetics. Part A.

A Novel Mutation in a Fijian Boy With Shwachman-Diamond Syndrome

Janet M. Yoon, B. Moghaddam, Aimee R Newman, 2009, Journal of pediatric hematology/oncology.

Recurrent HERV‐H‐Mediated 3q13.2–q13.31 Deletions Cause a Syndrome of Hypotonia and Motor, Language, and Cognitive Delays

J. Rosenfeld, L. Shaffer, P. Stankiewicz, 2013, Human mutation.