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Genotype-phenotype correlation in 27 pediatric patients in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a single center.
Yoo, Yangho; Chang, Mi Sun; Lee, Jieun; Cho, Sung Yoon; Park, Sung Won; Jin, Dong-Kyu; Park, Hyung-Doo.
Afiliación
  • Yoo Y; Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Chang MS; Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Lee J; Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Cho SY; Department of Pediatrics, Hanyang University Guri Hopistal, Hanyang University College of Medicine, Guri, Korea.
  • Park SW; Department of Pediatrics, Cheil General Hospital & Woman's Healthcare Center, Kwandong University College of Medicine, Seoul, Korea.
  • Jin DK; Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Park HD; Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Ann Pediatr Endocrinol Metab ; 18(3): 128-34, 2013 Sep.
Article en En | MEDLINE | ID: mdl-24904866
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Observational_studies Idioma: En Revista: Ann Pediatr Endocrinol Metab Año: 2013 Tipo del documento: Article Pais de publicación:
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Observational_studies Idioma: En Revista: Ann Pediatr Endocrinol Metab Año: 2013 Tipo del documento: Article Pais de publicación: