Ankyloblepharon-ectodermal Defects-cleft Lip-palate Syndrome Due to a Novel Missense Mutation in the SAM Domain of the <i>TP63</i> Gene.

Tajir, M; Lyahyai, J; Guaoua, S; El Alloussi, M; Sefiani, A

Ankyloblepharon-ectodermal Defects-cleft Lip-palate Syndrome Due to a Novel Missense Mutation in the SAM Domain of the TP63 Gene.

Tajir, M; Lyahyai, J; Guaoua, S; El Alloussi, M; Sefiani, A.

Tajir M; Research team in genomics and molecular epidemiology of genetic diseases, Genomics Center of Human Pathologies, Faculty of Medicine and Pharmacy, University Mohammed V, Rabat, Morocco.
Lyahyai J; Department of Medical Genetics, National Institute of Health, Rabat, Morocco.
Guaoua S; Medical Genetics Laboratory, Faculty of Medicine and Pharmacy, Mohamed Premier University, Oujda, Morocco.
El Alloussi M; Research team in genomics and molecular epidemiology of genetic diseases, Genomics Center of Human Pathologies, Faculty of Medicine and Pharmacy, University Mohammed V, Rabat, Morocco.
Sefiani A; Department of Medical Genetics, National Institute of Health, Rabat, Morocco.

Balkan J Med Genet ; 23(1): 95-98, 2020 Jun.

Article en En | MEDLINE | ID: mdl-32953416

Palabras clave

Ankyloblepharon; Congenital ectodermal defect and clefting; Hay-Wells syndrome; Sterile alpha motif (SAM) domain; TP63 gene

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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies / Screening_studies Idioma: En Año: 2020 Tipo del documento: Article

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Texto completo: 1 Banco de datos: MEDLINE Tipo de estudio: Prognostic_studies / Screening_studies Idioma: En Año: 2020 Tipo del documento: Article