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UnknownMutations in TSPEAR, Encoding a Regulator of Notch Signaling, Affect Tooth and Hair Follicle Morphogenesis.
Not available
S-EPMC5065119 | biostudies-literature
UnknownThe Role of Desmoglein 1 in Gap Junction Turnover Revealed through the Study of SAM Syndrome.
Not available
S-EPMC7039747 | biostudies-literature
UnknownPhenotypic and Genotypic Characterization of 171 Patients with Syndromic Inherited Retinal Diseases Highlights the Importance of Genetic Testing for Accurate Clinical Diagnosis
Not available
S-EPMC12295353 | biostudies-literature
UnknownJoubert Syndrome in French Canadians and Identification of Mutations in CEP104.
Not available
S-EPMC4667103 | biostudies-literature
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