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pro vyhledávání: '"Ru-Yi Tu"'
Autor:
Hsiang-Yu Lin, Chung-Lin Lee, Sisca Fran, Ru-Yi Tu, Ya-Hui Chang, Dau-Ming Niu, Chia-Ying Chang, Pao Chin Chiu, Yen-Yin Chou, Hui-Pin Hsiao, Chia-Feng Yang, Meng-Che Tsai, Tzu-Hung Chu, Chih-Kuang Chuang, Shuan-Pei Lin
Publikováno v:
Journal of Personalized Medicine, Vol 11, Iss 11, p 1066 (2021)
Background: Beckwith-Wiedemann syndrome (BWS; OMIM 130650) is a rare overgrowth syndrome with tumor predisposition resulting from the abnormal expression or function of imprinted genes of the chromosome 11p15.5 imprinting gene cluster. The aim of thi
Externí odkaz:
https://doaj.org/article/f01d2bc62ccb4234afbbcffd5be938ca
Autor:
Ya-Hui Chang, Hui-Pin Hsiao, Meng Che Tsai, Chung-Lin Lee, Pao Chin Chiu, Chia-Feng Yang, Chih-Kuang Chuang, Chia-Ying Chang, Hsiang-Yu Lin, Tzu-Hung Chu, Yen Yin Chou, Sisca Fran, Dau-Ming Niu, Ru-Yi Tu, Shuan-Pei Lin
Publikováno v:
Journal of Personalized Medicine, Vol 11, Iss 1066, p 1066 (2021)
Journal of Personalized Medicine
Volume 11
Issue 11
Journal of Personalized Medicine
Volume 11
Issue 11
Background: Beckwith-Wiedemann syndrome (BWS
OMIM 130650) is a rare overgrowth syndrome with tumor predisposition resulting from the abnormal expression or function of imprinted genes of the chromosome 11p15.5 imprinting gene cluster. The aim of
OMIM 130650) is a rare overgrowth syndrome with tumor predisposition resulting from the abnormal expression or function of imprinted genes of the chromosome 11p15.5 imprinting gene cluster. The aim of
Epigenotype, genotype, and phenotype analysis of patients in Taiwan with Beckwith–Wiedemann syndrome
Autor:
Yi-Ning Su, Tzu-Hung Chu, Dau-Ming Niu, Hsi-Che Liu, Shuan-Pei Lin, Chih-Kuang Chuang, Hsiang-Yu Lin, Chih-Ping Chen, Ru-Yi Tu, Chia-Ying Chang, Yi-Ya Fang
Publikováno v:
Molecular Genetics and Metabolism. 119:8-13
Beckwith-Wiedemann syndrome (BWS) is a congenital overgrowth disorder predisposing to tumorigenesis that results from abnormal expression or function of imprinted genes of chromosome 11p15.5.Forty-seven patients in Taiwan with clinical suspicion of B