Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Yi-Nin Su"'
Autor:
Shu-Chen Wei, Yen-Hsuan Ni, Hwai-I. Yang, Yi-Nin Su, Ming-Chu Chang, Yu-Ting Chang, Ming-Jium Shieh, Cheng-Yi Wang, Jau-Min Wong
Publikováno v:
Journal of the Formosan Medical Association, Vol 110, Iss 9, Pp 600-606 (2011)
The aim of this study was to gain a better understanding of the current incidence of Crohn’s disease (CD) in Taiwan and examine its clinical/genetic characteristics because there has been a trend toward increased diagnosis in the Asia-Pacific area.
Externí odkaz:
https://doaj.org/article/510aa3e493c74658b22189f70b60ee5b
Autor:
Hwai I. Yang, Ming Chu Chang, Yi Nin Su, Yu-Ting Chang, Ming-Jium Shieh, Yen-Hsuan Ni, Shu-Chen Wei, Cheng Yi Wang, Jau-Min Wong
Publikováno v:
Journal of the Formosan Medical Association, Vol 110, Iss 9, Pp 600-606 (2011)
Background/Purpose The aim of this study was to gain a better understanding of the current incidence of Crohn’s disease (CD) in Taiwan and examine its clinical/genetic characteristics because there has been a trend toward increased diagnosis in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76a5b6e1a77bffba1685adfc8277b4cf
Publikováno v:
Audiology and Neurotology. 15:311-317
Preimplantation genetic diagnosis (PGD) is used to analyze embryos genetically before their transfer into the uterus. For families with genetic diseases, PGD offers a chance to have an unaffected child, without facing termination of pregnancy. Althou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16684065ba687ab801c479495070bf38
https://doi.org/10.1159/000284349
https://doi.org/10.1159/000284349
Autor:
Chen-Chi Wu, Pei-Jer Chen, Yi-Nin Su, Chuan-Jen Hsu, Po-Lin Yeh, Ying-Chang Lu, Wuh-Liang Hwu
Publikováno v:
Audiology and Neurotology. 15:57-66
Recessive mutations in the SLC26A4 gene are responsible for nonsyndromic enlarged vestibular aqueduct (EVA) and Pendred syndrome. However, in some affected families, only 1 or 0 mutated allele can be identified, as well as no clear correlation betwee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7965b1cacdeb84cfcfdec6caf0ac77c8
https://doi.org/10.1159/000231567
https://doi.org/10.1159/000231567
Publikováno v:
Audiologyneuro-otology. 15(5)
Preimplantation genetic diagnosis (PGD) is used to analyze embryos genetically before their transfer into the uterus. For families with genetic diseases, PGD offers a chance to have an unaffected child, without facing termination of pregnancy. Althou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9cfc97aed036f0dbc72e94ee7b412d16
https://pubmed.ncbi.nlm.nih.gov/20160438
https://pubmed.ncbi.nlm.nih.gov/20160438
Autor:
Chen-Chi, Wu, Ying-Chang, Lu, Pei-Jer, Chen, Po-Lin, Yeh, Yi-Nin, Su, Wuh-Liang, Hwu, Chuan-Jen, Hsu
Publikováno v:
Audiologyneuro-otology. 15(1)
Recessive mutations in the SLC26A4 gene are responsible for nonsyndromic enlarged vestibular aqueduct (EVA) and Pendred syndrome. However, in some affected families, only 1 or 0 mutated allele can be identified, as well as no clear correlation betwee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d188d6ce5e6361b309727b05061cc920
https://pubmed.ncbi.nlm.nih.gov/19648736
https://pubmed.ncbi.nlm.nih.gov/19648736
Publikováno v:
Audiology & Neurotology; 2010, Vol. 15 Issue 5, p311-317, 7p, 1 Chart, 3 Graphs
Autor:
Chen-Chi Wu, Ying-Chang Lu, Pei-Jer Chen, Po-Lin Yeh, Yi-Nin Su, Wuh-Liang Hwu, Chuan-Jen Hsu
Publikováno v:
Audiology & Neurotology; 2010, Vol. 15 Issue 1, p57-66, 10p, 6 Charts, 1 Graph