Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: Abnormalities and FANCA[original query] |
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Evaluation of Fanconi Anemia genes in familial breast cancer predisposition. Cancer research 2003 12 63 (24): 8596-9. Seal Sheila, Barfoot Rita, Jayatilake Hiran, Smith Paula, Renwick Anthony, Bascombe Linda, McGuffog Lesley, Evans D Gareth, Eccles Diana, Easton Douglas F, Stratton Michael R, Rahman Nazneen, |
A novel duplication polymorphism in the FANCA promoter and its association with breast and ovarian cancer. BMC cancer 2005 5 (1): 43. Thompson Ella, Dragovic Rebecca L, Stephenson Sally-Anne, Eccles Diana M, Campbell Ian G, Dobrovic Alexand |
FANCA and FANCG are the major Fanconi anemia genes in the Korean population. Clinical genetics 2013 Sep 84 (3): 271-5. Park J, Chung N-G, Chae H, Kim M, Lee S, Kim Y, Lee J-W, Cho B, Jeong D C, Park I |
A rare FANCA gene variation as a breast cancer susceptibility allele in an Iranian population. Molecular medicine reports 2017 Apr . Abbasi Sakineh, Rasouli Mi |
Functional analysis of Fanconi anemia mutations in China. Experimental hematology 2018 7 66 32-41.e8. Li Niu, Ding Lixia, Li Benshang, Wang Jian, D'Andrea Alan D, Chen Ji |
Novel FANCA mutation in the first fully-diagnosed patient with Fanconi anemia in Polish population - case report. Molecular cytogenetics 2020 8 13 33. Repczynska Anna, Pastorczak Agata, Babol-Pokora Katarzyna, Skalska-Sadowska Jolanta, Drozniewska Malgorzata, Mlynarski Wojciech, Haus Ol |
A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjects. Human mutation 2021 Sep . George Merin, Solanki Avani, Chavan Niranjan, Rajendran Aruna, Raj Revathi, Mohan Sheila, Nemani Sandeep, Kanvinde Shailesh, Munirathnam Deendayalan, Rao Sudha, Radhakrishnan Nita, Lashkari Harsha Prasada, Ghildhiyal Radha Gulati, Manglani Mamta, Shanmukhaiah Chandrakala, Bhat Sunil, Ramesh Sowmyashree, Cherian Anchu, Junagade Pritesh, Vundinti Babu R |
Clinical, cytogenetic and molecular findings in nine Moroccan patients with Fanconi anemia. The Pan African medical journal 2021 8 39 72. Doubaj Yassamine, Zrhidri Abdelali, Elalaoui Siham Chafai, Lyahyai Jaber, El Kadiri Youssef, Elkassimi Nadia, Sbiti Aziza, El Kababri Maria, Hessissen Laila, Sefiani Abdelaz |
Nitric oxide synthase-2 (NOS2) gene polymorphism c.1832C>T (Ser608Leu) associated with nitrosative stress in Fanconi anaemia. Molecular biology reports 2021 Mar . George Merin, Solanki Avani, Mohanty Purvi, Dhangar Somprakash, Rajendran Aruna, Mohan Sheila, Vundinti Babu R |
Advances in genomic diagnosis of a large cohort of Egyptian patients with disorders of sex development. American journal of medical genetics. Part A 2021 3 185 (6): 1666-1677. Mazen Inas, Mekkawy Mona, Kamel Alaa, Essawi Mona, Hassan Heba, Abdel-Hamid Mohamed, Amr Khalda, Soliman Hala, El-Ruby Mona, Torky Ahmed, El Gammal Mona, Elaidy Aya, Bashamboo Anu, McElreavey Kenne |
Fanconi anemia gene-associated germline predisposition in aplastic anemia and hematologic malignancies. Frontiers of medicine 2021 Nov . Nie Daijing, Zhang Jing, Wang Fang, Li Xvxin, Liu Lili, Zhang Wei, Cao Panxiang, Chen Xue, Zhang Yang, Chen Jiaqi, Ma Xiaoli, Zhou Xiaosu, Wu Qisheng, Liu Ming, Liu Mingyue, Tian Wenjun, Liu Hongxi |
Severe telomere shortening in Fanconi anemia complementation group L. Molecular biology reports 2021 1 48 (1): 585-593. Shah Anjali, George Merin, Dhangar Somprakash, Rajendran Aruna, Mohan Sheila, Vundinti Babu R |
Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort. Haematologica 2022 4 108 (1): 69-82. Altintas Burak, Giri Neelam, McReynolds Lisa J, Best Ana, Alter Blanche |
Phenotypic and genotypic correlation evaluation of 148 pediatric patients with Fanconi anemia in a Chinese rare disease cohort. Clinica chimica acta; international journal of clinical chemistry 2022 12 539 41-49. Chang Lixian, Zhang Li, An Wenbin, Wan Yang, Cai Yuli, Lan Yang, Zhang Aoli, Liu Lipeng, Ruan Min, Liu Xiaoming, Guo Ye, Yang Wenyu, Chen Xiaojuan, Chen Yumei, Wang Shuchun, Zou Yao, Yuan Weiping, Zhu Xiaof |
Germ line variants in patients with acute myeloid leukemia without a suspicion of hereditary hematologic malignancy syndrome. Blood advances 2023 7 . Francesca Guijarro, Mònica López-Guerra, Jordi Morata, Alex Bataller, Sara Paz, Josep Maria Cornet-Masana, Antònia Banús-Mulet, Laia Cuesta-Casanovas, Josep Maria Carbó, Sandra Castaño-Díez, Carlos Jiménez-Vicente, Albert Cortés-Bullich, Ana Triguero, Alexandra Martínez-Roca, Daniel Esteban, Marta Gómez-Hernando, José Ramón Álamo Moreno, Irene López-Oreja, Marta Garrote, Ruth Muñoz Risueño, Raul Tonda, Ivo G Gut, Dolors Colomer, Marina Díaz-Beya, Jordi Este |
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- Page last updated:Apr 29, 2024
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