Characterizing facial features in individuals with craniofacial microsomia: A systematic approach for clinical research

Reliable classification of facial phenotypic variation in craniofacial microsomia: a comparison of physical exam and photographs

(2016) Craig B. Birgfeld et al.   Head & Face Medicine

Clarifying the Relationships among the Different Features of the OMENS+ Classification in Craniofacial Microsomia

(2015) A. Jorien Tuin et al.   PLASTIC AND RECONSTRUCTIVE SURGERY

Delineation ofEFTUD2Haploinsufficiency-Related Phenotypes Through a Series of 36 Patients

(2014) Daphné Lehalle et al.   HUMAN MUTATION

Oculoauriculofrontonasal syndrome: Case series revealing new bony nasal anomalies in an old syndrome

(2013) Kelly N. Evans et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Haploinsufficiency of a Spliceosomal GTPase Encoded by EFTUD2 Causes Mandibulofacial Dysostosis with Microcephaly

(2012) Matthew A. Lines et al.   AMERICAN JOURNAL OF HUMAN GENETICS

“Mandibulofacial dysostosis with microcephaly” caused byEFTUD2mutations: Expanding the phenotype

(2012) Daniela V. Luquetti et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Neurodevelopmental Outcomes in Children With Hemifacial Microsomia

(2011) Brent R. Collett et al.   ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE

A Phenotypic Assessment Tool for Craniofacial Microsomia

(2011) Craig B. Birgfeld et al.   PLASTIC AND RECONSTRUCTIVE SURGERY

Photographic protocol for image acquisition in craniofacial microsomia

(2011) Carrie L. Heike et al.   Head & Face Medicine

Characterizing the oculoauriculofrontonasal syndrome

(2009) Michael T. Gabbett et al.   CLINICAL DYSMORPHOLOGY