Associated Papers
Alternative lengthening of telomeres phenotype and loss of ATRX expression in sarcomas.
Ren X et al.
Oncology Letters, 2018
Prevalence of erythrocyte haemoglobin H inclusions in unselected patients with clonal myeloid disorders.
Steensma DP et al.
British Journal of Haematology, 2007
A new detection method for ATRX gene mutations using a mismatch-specific endonuclease.
Wada T et al.
American Journal of Medical Genetics. Part A, 2006
Mutations in PHD-like domain of the ATRX gene correlate with severe psychomotor impairment and severe urogenital abnormalities in patients with ATRX syndrome.
Badens C et al.
Clinical Genetics, 2006
Molecular-clinical spectrum of the ATR-X syndrome.
Gibbons RJ et al.
American Journal of Medical Genetics, 2000
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