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The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|May 21, 2004
Transverse craniofacial features and their genetic predisposition in families with nonsyndromic unilateral cleft lip and palateYoung-Jooh Yoon, Marja R Perkiomaki, Ross H Tallents, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|August 29, 2003
Association of nasomaxillary asymmetry in children with unilateral cleft lip and palate and their parentsYoung-Jooh Yoon, Marja R Perkiomaki, Ross H Tallents, et al.
Medical Education Online|December 23, 2011
Process of discovery: a fourth-year translational science courseBenedict F DiGiovanni, Denham S Ward, Steven M O'Donnell, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 9, 2003
Association of distinct craniofacial features in nonsyndromic cleft lip and palate family membersMarja R Perkiomaki, Young-Jooh Yoon, Ross H Tallents, et al.
Molecular Genetics and Metabolism|March 27, 2014
Sapropterin dihydrochloride use in pregnant women with phenylketonuria: an interim report of the PKU MOMS sub-registryDorothy K Grange, Richard E Hillman, Barbara K Burton, et al.
Hearing Research|October 30, 2012
GRM7 variants associated with age-related hearing loss based on auditory perceptionDina L Newman, Laurel M Fisher, Jeffrey Ohmen, et al.
Reproductive Sciences (Thousand Oaks, Calif.)|January 27, 2011
Single-nucleotide polymorphisms in the KCNN3 gene associate with preterm birthLori J Day, Kendra L Schaa, Kelli K Ryckman, et al.
American Journal of Medical Genetics. Part A|December 9, 2022
Perspectives on the future of dysmorphologyBenjamin D Solomon, Margaret P Adam, Chin-To Fong, et al.
Pediatric Research|November 22, 2012
Candidate gene linkage approach to identify DNA variants that predispose to preterm birthElise N A Bream, Cara R Leppellere, Margaret E Cooper, et al.
Genome Medicine|September 30, 2022
Sequencing individual genomes with recurrent genomic disorder deletions: an approach to characterize genes for autosomal recessive rare disease traitsBo Yuan, Katharina V Schulze, Nurit Assia Batzir, et al.
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