[Screening of phenylketonuria and analysis of phenylalanine hydroxylase gene in 380 996 newborns from Hainan province].

Zhao, Z D; Huang, C D; Xu, H Z; Fu, C H

Zhao, Z D; Huang, C D; Xu, H Z; Fu, C H.

Afiliación

Zhao ZD; Neonatal Disease Screening Center, Hainan Women and Children's Medical Center, Haikou 570206, China.
Huang CD; Neonatal Disease Screening Center, Hainan Women and Children's Medical Center, Haikou 570206, China.
Xu HZ; Neonatal Disease Screening Center, Hainan Women and Children's Medical Center, Haikou 570206, China.
Fu CH; Neonatal Disease Screening Center, Hainan Women and Children's Medical Center, Haikou 570206, China.

Zhonghua Yi Xue Za Zhi ; 100(26): 2054-2058, 2020 Jul 14.

Article en Zh | MEDLINE | ID: mdl-32654453

Asunto(s)

Fenilalanina Hidroxilasa/genética; Fenilcetonurias/genética; Alelos; Femenino; Humanos; Recién Nacido; Masculino; Tamizaje Masivo; Mutación

Palabras clave

Incidence; Infant, newborn; Phenylalanine hydroxylase; Phenylketonurias

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenilalanina Hidroxilasa / Fenilcetonurias Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Female / Humans / Male / Newborn Idioma: Zh Revista: Zhonghua Yi Xue Za Zhi Año: 2020 Tipo del documento: Article País de afiliación: China

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