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MatchTypeWhy
Craniofacial AbnormalitiesConcept Why?
Clouthier, DavidPerson Why?
Bilateral Ear Canal Cholesteatoma with Underlying Type I First Branchial Cleft Anomalies.Academic Article Why?
Loss-of-function of Endothelin receptor type A results in Oro-Oto-Cardiac syndrome.Academic Article Why?
Smith, FrancisPerson Why?
TASP1 mutation in a female with craniofacial anomalies, anterior segment dysgenesis, congenital immunodeficiency and macrocytic anemia.Academic Article Why?
The Society for Craniofacial Genetics and Developmental Biology 42nd Annual Meeting.Academic Article Why?
The society for craniofacial genetics and developmental biology 43rd annual meeting.Academic Article Why?
Artinger, KristinPerson Why?
Shull, LomeliPerson Why?
A Novel Approach to Dysmorphology to Enhance the Phenotypic Classification of Autism Spectrum Disorder in the Study to Explore Early Development.Academic Article Why?
A tissue-specific role for intraflagellar transport genes during craniofacial development.Academic Article Why?
Characteristics of children under 2 years of age undergoing tonsillectomy for upper airway obstruction.Academic Article Why?
Composite tissue allotransplantation for the reconstruction of congenital craniofacial defects.Academic Article Why?
Developmental pathogenesis of short palpebral fissure length in children with fetal alcohol syndrome.Academic Article Why?
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