MYT1 role in the microtia‐craniofacial microsomia spectrum

Background Craniofacial microsomia (CFM), also known as the oculo‐auriculo‐vertebral spectrum, comprises a variable phenotype with the most common features including microtia and mandibular hypoplasia on one or both sides, in addition to lateral oral clefts, epibulbar dermoids, cardiac, vertebral, a...

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Veröffentlicht in:	Molecular genetics & genomic medicine 2020-10, Vol.8 (10), p.e1401-n/a, Article 1401
Hauptverfasser:	Luquetti, Daniela V., Heike, Carrie L., Zarante, Ignacio, Timms, Andrew E., Gustafson, Jonas, Pachajoa, Harry, Porras‐Hurtado, Gloria L., Ayala‐Ramirez, Paola, Duenas‐Roque, Milagros M., Jimenez, Natalia, Ibanez, Lina M., Hurtado‐Villa, Paula
Format:	Artikel
Sprache:	eng
Schlagworte:	Abnormalities Birth weight Clinical Report Clinical Reports craniofacial microsomia Deoxyribonucleic acid DNA Etiology Families & family life Gene sequencing Genetic analysis genetics Genetics & Heredity Genomes Genotype & phenotype Genotypes Haplotypes Hearing loss hemifacial microsomia Hypoplasia Life Sciences & Biomedicine Microtia Mutation oculo‐auriculo‐vertebral spectrum Phenotypes Science & Technology Vertebrae
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