Arama Sonuçları - "mutation"

MEFV mutations in systemic JIA Yazar: Aktay Ayaz N, Bilginer Y, Yilmaz E, Ergüven M, Topaloglu R, Bakkaloglu A, Ozen S

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CHRNE Mutation and Congenital Myasthenia Yazar: J Gordon Millichap

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Poikiloderma with novel gene mutation Yazar: Sunanda Mahajan, Anuja Sunkwad, Bhushan Darkase, Uday Khopkar

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Class 1 CF Mutations Yazar: Michael eWilschanski

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Fragile X Mutations and Epilepsy Yazar: J Gordon Millichap

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Molecular variants and mutations in medulloblastoma Yazar: Schroeder K, Gururangan S

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Characterization of KIT mutation in melanoma Yazar: Chi-Yuan Tzen, Yu-Hung Wu, Chin-Yuan Tzen

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Biotechnologies for Plant Mutation Breeding Protocols

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Species and Varieties, Their Origin by Mutation Yazar: Vries, Hugo de, 1848-1935; MacDougal, Daniel Trembly, 1865-1958 [Editor]

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High tumor mutation burden is associated with DNA damage repair gene mutation in breast carcinomas Yazar: Ping Mei, C. Eric Freitag, Lai Wei, Yunxiang Zhang, Anil V. Parwani, Zaibo Li

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Evaluation of ataxia-telangiectasia mutated IVS10 mutation in breast cancer along with clinicopathological parameters Yazar: Sana Ahuja, Himani Aneja, Amit Kumar Yadav, Sunil Ranga, Chintamani, Jaishree Paul

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Mutation spectrum of Kallmann syndrome: identification of five novel mutations across ANOS1 and FGFR1 Yazar: Guoming Chu, Pingping Li, Qian Zhao, Rong He, Yanyan Zhao

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Expanding the mutational spectrum of monogenic hypogonadotropic hypogonadism: novel mutations in ANOS1 and FGFR1 genes Yazar: Agnieszka Gach, Iwona Pinkier, Maria Szarras-Czapnik, Agata Sakowicz, Lucjusz Jakubowski

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Not BCL2 mutation but dominant mutation conversation contributed to acquired venetoclax resistance in acute myeloid leukemia Yazar: Xiang Zhang, Jiejing Qian, Huafeng Wang, Yungui Wang, Yi Zhang, Pengxu Qian, Yinjun Lou, Jie Jin, Honghu Zhu

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Ataxia-telangiectasia mutated (ATM) gene mutation in a patient with primary cutaneous marginal zone lymphoma Yazar: Melissa M. Sarver, BS, Kimberly F. Breglio, MD, DPhil, Elise A. Olsen, MD

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IDH1 mutated low grade astrocytoma occurring in MSH2 mutated Lynch syndrome family Yazar: Alaa Alkhotani, Ingrid Ambus, Lea Velsher, Corwyn Rowsell, Julia Keith

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Compound Heterozygous Mutations Involving Splicing Mutations Cause Rothmund-Thomson Syndrome in Two Chinese Families Yazar: Chao-Lan Pan, Qiao-Yu Cao, Yue Li, Jia Zhang, Zhen Zhang, Yu-Meng Wang, Fu-Ying Chen, Ru-Hong Cheng, Xiao-Xiao Wang, Zhi-Rong Yao, Zhi-Yong Lu, Ming Li

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Le genre face aux mutations Yazar: Luc Capdevila, Sophie Cassagnes, Martine Cocaud, Dominique Godineau, François Rouquet, Jacqueline Sainclivier (dir.)

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L'économie cistercienne : Géographie. Mutations Yazar: Charles Higounet

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Les mutations de l'écriture Yazar: François Nicolas (dir.)

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