Fanconi-like anemia related to a FANCM mutation
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference17 articles.
1. Biallelic truncating FANCM mutations cause early-onset cancer but not Fanconi anemia;Bogliolo;Genet. Med.,2018
2. Optimised molecular genetic diagnostics of Fanconi anaemia by whole exome sequencing and functional studies;Bogliolo;J. Med. Genet.,2020
3. A common founder mutation in FANCA underlies the world's highest prevalence of Fanconi anemia in Gypsy families from Spain;Callén;Blood,2005
4. A common founder mutation in FANCA underlies the world's highest prevalence of Fanconi anemia in Gypsy families from Spain;Callén;Blood,2005
5. [Molecular basis of Fanconi's anemia];Digweed;Klin. Pädiatr.,1999
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1. FANCM Gene Variants in a Male Diagnosed with Sertoli Cell-Only Syndrome and Diffuse Astrocytoma;Genes;2024-05-28
2. Grade 5 Radiation Necrosis After Whole-Brain Radiation Therapy;Practical Radiation Oncology;2024-03
3. Myelodysplastic syndrome and multiple solid tumours in an individual with compound heterozygous deleterious FANCM variants: A case report and review of the literature;British Journal of Haematology;2023-08-22
4. Fancm has dual roles in the limiting of meiotic crossovers and germ cell maintenance in mammals;Cell Genomics;2023-08
5. Fancm regulates meiotic double-strand break repair pathway choice in mammals;2022-06-17
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