Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Syndrome and MAPK1[original query] |
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A clinical scoring system for selection of patients for PTEN mutation testing is proposed on the basis of a prospective study of 3042 probands. American journal of human genetics 2011 1 88 (1): 42-56. Tan Min-Han, Mester Jessica, Peterson Charissa, Yang Yiran, Chen Jin-Lian, Rybicki Lisa A, Milas Kresimira, Pederson Holly, Remzi Berna, Orloff Mohammed S, Eng Char |
Genetic Variants Within Molecular Targets of Antipsychotic Treatment: Effects on Treatment Response, Schizophrenia Risk, and Psychopathological Features. Journal of molecular neuroscience : MN 2017 Nov . Calabrò Marco, Porcelli Stefano, Crisafulli Concetta, Wang Sheng-Min, Lee Soo-Jung, Han Changsu, Patkar Ashwin A, Masand Prakash S, Albani Diego, Raimondi Ilaria, Forloni Gianluigi, Bin Sofia, Cristalli Carlotta, Mantovani Vilma, Pae Chi-Un, Serretti Alessand |
Idiopathic hypereosinophilia is clonal disorder? Clonality identified by targeted sequencing. PloS one 2017 12 (10): e0185602. Lee Jee-Soo, Seo Heewon, Im Kyongok, Park Si Nae, Kim Sung-Min, Lee Eun Kyoung, Kim Jung-Ah, Lee Joon-Hee, Kwon Sunghoon, Kim Miyoung, Koh Insong, Hwang Seungwoo, Park Heung-Woo, Kang Hye-Ryun, Park Kyoung Soo, Kim Ju Han, Lee Dong So |
Comprehensive analysis of mutations of renal cell carcinoma in an autosomal dominant polycystic kidney disease patient. Medicine 2020 5 99 (19): e20071. Shim Kwang Eon, Lee Chung, Kim Jin Up, Choi Gwang Ho, Kwak Kyoung Min, Kim Seok Hyung, Kim Hyunho, Yoon Jong Woo, Shin Tae Young, Jeong Chang Wook, Kim Hyuns |
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