Michael L. Begleiter

The genetic basis of DOORS syndrome: an exome-sequencing study

Philippe M. Campeau, Dalia Kasperavičiūtė, James T. Lu et al. · The Lancet Neurology · 2013 · 227 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Reproductive risk of t(13q14q) carriers: Case report and review

D. James Harris, L. Hankins, Michael L. Begleiter et al. · American Journal of Medical Genetics · 1979 · 101 citations

Life Sciences, Genetics, Molecular Genetics +15

Parental trisomy 21 mosaicism.

D. James Harris, Michael L. Begleiter, John Chamberlin et al. · PubMed · 1982 · 42 citations

Life Sciences, Genetics, Molecular Genetics +12

Mutations in the Histone Modifier PRDM6 Are Associated with Isolated Nonsyndromic Patent Ductus Arteriosus

Na Li, Lakshman Subrahmanyan, Emily Smith et al. · The American Journal of Human Genetics · 2016 · 38 citations · Full text

Medicine, Genetics, Molecular Genetics +11

Expanding the phenotype of oculoectodermal syndrome: Possible relationship to encephalocraniocutaneous lipomatosis

Holly H Ardinger, Kimberly A. Horii, Michael L. Begleiter · American Journal of Medical Genetics Part A · 2007 · 37 citations

Medicine, Ophthalmology, Pathology +4