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Robustness of Distinctive Facial Features in Prader-Willi Syndrome: A Stereophotogrammetric Analysis and Association with Clinical and Biochemical Markers in Adult Individuals

Background: Prader-Willi syndrome (PWS) is a rare genomic imprinting disorder associated to a complex neurodevelopmental phenotype and a distinctive facial appearance. The study investigated the relationships between the quantitative facial dysmorphism in PWS and clinical and biochemical markers of...

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Egile Nagusiak: Claudia Dolci, Antonello E. Rigamonti, Annalisa Cappella, Daniele M. Gibelli, Graziano Grugni, Diana Caroli, Chiarella Sforza, Alessandro Sartorio
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: MDPI AG 2022-07-01
Saila:Biology
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Sarrera elektronikoa:https://www.mdpi.com/2079-7737/11/8/1148
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