HuGE Literature Finder
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Novel Bi-Allelic Variants of FANCM Cause Sertoli Cell-Only Syndrome and Non-Obstructive Azoospermia. Frontiers in genetics 2022 1 12 799886. Zhang Yuxiang, Li Peng, Liu Nachuan, Jing Tao, Ji Zhiyong, Yang Chao, Zhao Liangyu, Tian Ruhui, Chen Huixing, Huang Yuhua, Zhi Erlei, Ou Ningjing, Bai Haowei, Zhou Yuchuan, Li Zheng, Yao Chenche |
Biallelic truncating FANCM mutations cause early-onset cancer but not Fanconi anemia. Genetics in medicine : official journal of the American College of Medical Genetics 2017 8 20 (4): 458-463. Bogliolo Massimo, Bluteau Dominique, Lespinasse James, Pujol Roser, Vasquez Nadia, d'Enghien Catherine Dubois, Stoppa-Lyonnet Dominique, Leblanc Thierry, Soulier Jean, Surrallés Jor |
Mutational analysis of FANCL, FANCM and the recently identified FANCI suggests that among the 13 known Fanconi Anemia genes, only FANCD1/BRCA2 plays a major role in high-risk breast cancer predisposition. Carcinogenesis 2009 Nov 30 (11): 1898-902. García María J, Fernández Victoria, Osorio Ana, Barroso Alicia, Fernández Fernando, Urioste Miguel, Benítez Javi |
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