[Screening results and genetic analysis of neonatal tetrahydrobiopterin deficiency in Hainan Province from 2007 to 2019].

Huang, C D; Zhao, Z D; Liu, X L; Wen, Y M; Haizhu, H Z; Zhu, X M; Yang, C; Wang, J

Huang, C D; Zhao, Z D; Liu, X L; Wen, Y M; Haizhu, H Z; Zhu, X M; Yang, C; Wang, J.

Afiliación

Huang CD; Neonatal Disease Screening Center, Hainan Women's and Children's Medical Center, Haikou 570206, China.
Zhao ZD; Neonatal Disease Screening Center, Hainan Women's and Children's Medical Center, Haikou 570206, China.
Liu XL; Neonatal Disease Screening Center, Hainan Women's and Children's Medical Center, Haikou 570206, China.
Wen YM; Neonatal Disease Screening Center, Hainan Women's and Children's Medical Center, Haikou 570206, China.
Haizhu HZ; Neonatal Disease Screening Center, Hainan Women's and Children's Medical Center, Haikou 570206, China.
Zhu XM; Neonatal Disease Screening Center, Hainan Women's and Children's Medical Center, Haikou 570206, China.
Yang C; Neonatal Disease Screening Center, Hainan Women's and Children's Medical Center, Haikou 570206, China.
Wang J; Neonatal Disease Screening Center, Hainan Women's and Children's Medical Center, Haikou 570206, China.

Zhonghua Yi Xue Za Zhi ; 101(38): 3161-3163, 2021 Oct 19.

Article en Zh | MEDLINE | ID: mdl-34674428

Asunto(s)

Fenilcetonurias; Femenino; Pruebas Genéticas; Humanos; Incidencia; Recién Nacido; Masculino; Tamizaje Masivo; Mutación; Fenilcetonurias/diagnóstico; Fenilcetonurias/epidemiología; Fenilcetonurias/genética

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fenilcetonurias Tipo de estudio: Diagnostic_studies / Incidence_studies / Prognostic_studies / Screening_studies Límite: Female / Humans / Male / Newborn Idioma: Zh Revista: Zhonghua Yi Xue Za Zhi Año: 2021 Tipo del documento: Article País de afiliación: China

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