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Pediatric Neurology|October 10, 2012
Epilepsy in Muenke syndrome: FGFR3-related craniosynostosisNneamaka B Agochukwu, Benjamin D Solomon, Andrea L Gropman, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 28, 2010
Cyclopia (synophthalmia) in Smith-Lemli-Opitz syndrome: First reported case and consideration of mechanismDavid D Weaver, Benjamin D Solomon, Kelly Akin-Samson, et al.Molecular Genetics and Metabolism|April 17, 2012
Molecular analysis of the Noggin (NOG) gene in holoprosencephaly patientsKshitij Srivastava, Ping Hu, Benjamin D Solomon, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 28, 2010
Holoprosencephaly flashcards: A summary for the clinicianBenjamin D Solomon, Daniel E Pineda-Alvarez, Sandra Mercier, et al.Clinical Dysmorphology|May 31, 2012
Holoprosencephaly-polydactyly/pseudotrisomy 13: a presentation of two new cases and a review of the literatureSophia M Bous, Benjamin D Solomon, Luitgard Graul-Neumann, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|April 8, 2014
Holoprosencephaly: ZIC2 mutation in a case with panhypopituitarismSener Tasdemir, Ibrahim Sahin, Atilla Cayır, et al.American Journal of Medical Genetics. Part A|April 9, 2009
A novel SIX3 mutation segregates with holoprosencephaly in a large familyBenjamin D Solomon, Felicitas Lacbawan, Mahim Jain, et al.Congenital Anomalies|April 15, 2003
The interplay of genetic and environmental factors in craniofacial morphogenesis: holoprosencephaly and the role of cholesterolRobin Edison, Maximilian MuenkePageof 29