Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: Syndrome and EGF[original query] |
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The relationship between the epidermal growth factor (EGF) 5'UTR variant A61G and melanoma/nevus susceptibility. The Journal of investigative dermatology 2004 Oct 123 (4): 755-9. Randerson-Moor J A, Gaut R, Turner F, Whitaker L, Barrett J H, Silva I dos Santos, Swerdlow A, Bishop D T, Bishop J A Newt |
Mutations in the EGF-CFC gene cryptic are an infrequent cause of congenital heart disease. Pediatric cardiology 0 27 (6): 695-8. Ozcelik Cemil, Bit-Avragim Nana, Panek Anna, Gaio Ursula, Geier Christian, Lange Peter E, Dietz Rainer, Posch Maximilian G, Perrot Andreas, Stiller Brigit |
Sex-specific association of epidermal growth factor gene polymorphisms with acute respiratory distress syndrome. The European respiratory journal 2009 Mar 33 (3): 543-50. Sheu C C, Zhai R, Su L, Tejera P, Gong M N, Thompson B T, Chen F, Christiani D |
Novel CRELD1 gene mutations in patients with atrioventricular septal defect. World journal of pediatrics : WJP 2010 Nov 6 (4): 348-52. Guo Ying, Shen Jie, Yuan Lang, Li Fen, Wang Jian, Sun K |
A maiden report on CRELD1 single-nucleotide polymorphism association in congenital heart disease patients of Mysore, South India. Genetic testing and molecular biomarkers 0 15 (7-8): 483-7. Kusuma Lingaiah, Dinesh Sosalagere M, Savitha Mysore R, Krishnamurthy Balasundaram, Narayanappa Doddaiah, Ramachandra Nallur |
Relationship between EGF, TGFA, and EGFR Gene Polymorphisms and Traditional Chinese Medicine ZHENG in Gastric Cancer. Evidence-based complementary and alternative medicine : eCAM 2013 2013 731071. Zhang Junfeng, Zhan Zhen, Wu Juan, Zhang Chunbing, Yang Yaping, Tong Shujuan, Wang Ruiping, Yang Xuewen, Dong Wei, Chen Yaj |
De Novo Coding Variants Are Strongly Associated with Tourette Disorder. Neuron 2017 May 94 (3): 486-499.e9. Willsey A Jeremy, Fernandez Thomas V, Yu Dongmei, King Robert A, Dietrich Andrea, Xing Jinchuan, Sanders Stephan J, Mandell Jeffrey D, Huang Alden Y, Richer Petra, Smith Louw, Dong Shan, Samocha Kaitlin E, , , Neale Benjamin M, Coppola Giovanni, Mathews Carol A, Tischfield Jay A, Scharf Jeremiah M, State Matthew W, Heiman Gary |
CRELD1 gene variants and atrioventricular septal defects in Down syndrome. Gene 2017 10 641 180-185. Asim Ambreen, Agarwal Sarita, Panigrahi Inusha, Sarangi Aditya Narayan, Muthuswamy Srinivasan, Kapoor Adit |
Modulation of Apoptosis by Cytotoxic Mediators and Cell-Survival Molecules in Sjögren's Syndrome. International journal of molecular sciences 2018 8 19 (8): . Nakamura Hideki, Horai Yoshiro, Shimizu Toshimasa, Kawakami Atsus |
Serum Epidermal Growth Factor is Low in Schizophrenia and Not Affected by Antipsychotics Alone or Combined With Electroconvulsive Therapy. Frontiers in psychiatry 2020 3 11 104. Zhang Xiaobin, Xiao Wenhuan, Chen KuanYu, Zhao Yaqin, Ye Fei, Tang Xiaowei, Du Xiangdo |
Classification and Interpretation for 11 FBN1 Variants Responsible for Marfan Syndrome and Pre-implantation Genetic Testing (PGT) for Two Families Successfully Blocked Transmission of the Pathogenic Mutations. Frontiers in molecular biosciences 2021 12 8 749842. Chen Songchang, Fei Hongjun, Zhang Junyun, Chen Yiyao, Huang Hefeng, Lu Daru, Xu Chenmi |
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- Page last updated:Apr 16, 2024
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