Human Genome Epidemiology Literature Finder
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Records 1 - 7 (of 7 Records) |
| Query Trace: Counseling and RET[original query] |
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| Polymerase chain reaction-single strand conformational polymorphism analysis of rearranged during transfection proto-oncogene in Chinese familial Hirschsprung's disease. World journal of gastroenterology 2005 1 11 (2): 275-9. Guan Tao, Li Ji-Cheng, Li Min-Ju, Tou Jin- |
| RET and EDNRB mutation screening in patients with Hirschsprung disease: Functional studies and its implications for genetic counseling. European journal of human genetics : EJHG 2015 Sep . Widowati Titis, Melhem Shamiram, Patria Suryono Y, de Graaf Bianca M, Sinke Richard J, Viel Martijn, Dijkhuis Jos, Sadewa Ahmad H, Purwohardjono Rochadi, Soenarto Yati, Hofstra Robert Mw, Sribudiani Yun |
| Presence of the RET Cys634Tyr mutation and Gly691Ser functional polymorphism in Iranian families with multiple endocrine neoplasia type 2A. Hormones (Athens, Greece) 2016 Jan . Aghdam Maryam Nasiri, Abbaszadegan Mohammad Reza, Tafazoli JAlireza, Aslzare Mohammad, Mosavi Zohr |
| A Brief Review on The Molecular Basis of Medullary Thyroid Carcinoma. Cell journal 2017 1 18 (4): 485-492. Mohammadi Masoumeh, Hedayati Meh |
| Utilization of Genetic Testing for RET Mutations in Patients with Medullary Thyroid Carcinoma: a Single-Center Experience. Journal of genetic counseling 2018 6 27 (6): 1411-1416. Parkhurst Emily, Calonico Elise, Abboy Sride |
| Prevalence of MET exon 14 skipping mutation in pulmonary sarcomatoid carcinoma patients without common targetable mutations: A single-institute study. Journal of cancer research and therapeutics 2019 15 (4): 909-913. Yu Yongfeng, Zhang Qing, Zhang Jie, Lu Sh |
| Germline BRCA1 Mutation Detected in a Multiple Endocrine Neoplasia Type 2 Case With RET Codon 634 Mutation. Frontiers in genetics 2019 7 10 544. Sarkadi Balázs, Baghy Kornélia, Sápi Zoltán, Nyir? Gábor, Likó István, Patócs Atti |
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