Concepedia

Margaret J. McMillin

MJ

3

Publications

323

Citations

3

H-Index

2012

Active since

Affiliations

University of Washington(Current)

Boston Children's Hospital

University of California, Irvine

Seattle Children's Hospital

Inserm

Margaret J. McMillin is an author at University of Washington specializing in medicine, genetics, and molecular genetics.

Top concepts

GeneticsMedicineMolecular GeneticsClinical DisordersCochlear DevelopmentDevelopmental Biology

Publications per year

2012–2015

3

Publications

3

De Novo Mutations in NALCN Cause a Syndrome Characterized by Congenital Contractures of the Limbs and Face, Hypotonia, and Developmental Delay

Jessica X. Chong, Margaret J. McMillin, Kathryn M. Shively et al. · The American Journal of Human Genetics · 2015 · 156 citations · Full text

Developmental Anomaly, Clinical Disorders, Developmental Biology +8

Mutations in KCTD1 Cause Scalp-Ear-Nipple Syndrome

Alexander G. Marneros, Anita E. Beck, Emily H. Turner et al. · The American Journal of Human Genetics · 2013 · 86 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +3

Mutations in ECEL1 Cause Distal Arthrogryposis Type 5D

Margaret J. McMillin, Jennifer E. Below, Kathryn M. Shively et al. · The American Journal of Human Genetics · 2012 · 81 citations · Full text

Genetic Disorder, Genetics, Molecular Genetics +3

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