Multimodality Craniofacial Phenotyping of Congenital Facial Weakness Disorders.

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Bibliographic Details
Title: Multimodality Craniofacial Phenotyping of Congenital Facial Weakness Disorders.
Authors: Almpani K; Craniofacial Anomalies and Regeneration Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MB, USA., Devine KR; Craniofacial Anomalies and Regeneration Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MB, USA., Liberton DK; Craniofacial Anomalies and Regeneration Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MB, USA., Mishra R; Craniofacial Anomalies and Regeneration Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MB, USA., Bassim C; Craniofacial Anomalies and Regeneration Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MB, USA., Van Ryzin C; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, Bethesda, MD, USA., Facio FM; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, Bethesda, MD, USA., Webb BD; Department of Genetics and Genomic Sciences and Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; Department of Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, WI, USA., Barry BJ; Department of Neurology, Boston Children's Hospital, Boston, MA, USA.; F.M. Kirby Neurobiology Center, Boston Children's Hospital, Boston, MA, USA.; Howard Hughes Medical Institute, Chevy Chase, MD, USA., Engle EC; Department of Neurology, Boston Children's Hospital, Boston, MA, USA.; Departments of Ophthalmology, Boston Children's Hospital and Harvard Medical School, Howard Hughes Medical Institute, Chevy Chase, Boston, MA, USA., Wang Jabs E; Department of Genetics and Genomic Sciences and Pediatrics, Icahn School of Medicine at Mount Sinai, New York, NY, USA.; Departments of Genetic Medicine and Pediatrics, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.; Department of Clinical Genomics, Mayo Clinic, Rochester, MN, USA., Collins FS; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, Bethesda, MD, USA.; Center for Precision Health Research, National Human Genome Research Institute, Bethesda, MD, USA., Manoli I; Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, Bethesda, MD, USA., Lee JS; Craniofacial Anomalies and Regeneration Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MB, USA.
Corporate Authors: Moebius Syndrome Research Consortium
Source: The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association [Cleft Palate Craniofac J] 2026 Jun; Vol. 63 (6), pp. 1455-1468. Date of Electronic Publication: 2025 Jul 03.
Publication Type: Journal Article
Journal Info: Publisher: SAGE Publications in Association with American Cleft Palate-Craniofacial Association Country of Publication: United States NLM ID: 9102566 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1545-1569 (Electronic) Linking ISSN: 10556656 NLM ISO Abbreviation: Cleft Palate Craniofac J Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1545-1569
DOI:10.1177/10556656251344128