Complete Labyrinthine Aplasia: A Unique Sign for Targeted Genetic Testing in Hearing Loss.

Lallar, Meenakshi; Arora, Veronica; Saxena, Renu; Puri, Ratna Dua; Verma, Ishwar Chander

Lallar, Meenakshi; Arora, Veronica; Saxena, Renu; Puri, Ratna Dua; Verma, Ishwar Chander.

Afiliación

Lallar M; Institute of Medical Genetics and Genomics, Sir Ganga Ram Hospital, New Delhi, India.
Arora V; Institute of Medical Genetics and Genomics, Sir Ganga Ram Hospital, New Delhi, India.
Saxena R; Institute of Medical Genetics and Genomics, Sir Ganga Ram Hospital, New Delhi, India.
Puri RD; Institute of Medical Genetics and Genomics, Sir Ganga Ram Hospital, New Delhi, India.
Verma IC; Institute of Medical Genetics and Genomics, Sir Ganga Ram Hospital, New Delhi, India.

J Pediatr Genet ; 10(1): 70-73, 2021 Mar.

Article en En | MEDLINE | ID: mdl-33552643

Palabras clave

FGF3 gene; LAMM; complete labyrinthine aplasia

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Pediatr Genet Año: 2021 Tipo del documento: Article País de afiliación: India Pais de publicación: Alemania

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