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A 23-Nucleotide Deletion in STK11 Gene Causes Peutz-Jeghers Syndrome and Malignancy in a Chinese Patient Without a Positive Family History.
Zhao, Zi-Ye; Jiang, Yu-Liang; Li, Bai-Rong; Yang, Fu; Li, Jing; Jin, Xiao-Wei; Ning, Shou-Bin; Sun, Shu-Han.
Afiliação
  • Zhao ZY; Department of Medical Genetics, Naval Medical University, 800 Xiangyin Rd., Shanghai, 200433, China.
  • Jiang YL; Department of Gastroenterology, Airforce General Hospital of PLA, 30 Fucheng Rd., Beijing, 100142, China.
  • Li BR; Department of Gastroenterology, Airforce General Hospital of PLA, 30 Fucheng Rd., Beijing, 100142, China.
  • Yang F; Department of Medical Genetics, Naval Medical University, 800 Xiangyin Rd., Shanghai, 200433, China.
  • Li J; Department of Gastroenterology, Airforce General Hospital of PLA, 30 Fucheng Rd., Beijing, 100142, China.
  • Jin XW; Department of Gastroenterology, Airforce General Hospital of PLA, 30 Fucheng Rd., Beijing, 100142, China.
  • Ning SB; Department of Gastroenterology, Airforce General Hospital of PLA, 30 Fucheng Rd., Beijing, 100142, China. ningshoubin@126.com.
  • Sun SH; Department of Medical Genetics, Naval Medical University, 800 Xiangyin Rd., Shanghai, 200433, China. shsun@vip.sina.com.
Dig Dis Sci ; 62(11): 3014-3020, 2017 11.
Article em En | MEDLINE | ID: mdl-28986664

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Peutz-Jeghers / Biomarcadores Tumorais / Deleção de Sequência / Proteínas Serina-Treonina Quinases Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Adult / Female / Humans País como assunto: Asia Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Peutz-Jeghers / Biomarcadores Tumorais / Deleção de Sequência / Proteínas Serina-Treonina Quinases Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies Limite: Adult / Female / Humans País como assunto: Asia Idioma: En Ano de publicação: 2017 Tipo de documento: Article