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Quoted phrase not found in phrase index: "Lung disease, immunodeficiency, and chromosome breakage syndrome;"
Page 1
Novel SMARCAL1 bi-allelic mutations associated with a chromosomal breakage phenotype in a severe SIOD patient.
Simon AJ, Lev A, Jeison M, Borochowitz ZU, Korn D, Lerenthal Y, Somech R. Simon AJ, et al. J Clin Immunol. 2014 Jan;34(1):76-83. doi: 10.1007/s10875-013-9957-3. Epub 2013 Nov 7. J Clin Immunol. 2014. PMID: 24197801
PURPOSE: Chromosomal instability syndromes include a group of rare diseases characterized by defective DNA-damage-response and increased risk of chromosomal breakage. Patients display defects in the recognition and/or repair of DNA damage, with a subsequent h …
PURPOSE: Chromosomal instability syndromes include a group of rare diseases characterized by defective DNA-damage-response and …
Chromosomal in-vitro radiosensitivity of lymphocytes in radiotherapy patients and AT-homozygotes.
Dunst J, Neubauer S, Becker A, Gebhart E. Dunst J, et al. Strahlenther Onkol. 1998 Oct;174(10):510-6. doi: 10.1007/BF03038983. Strahlenther Onkol. 1998. PMID: 9810318
PATIENTS AND METHODS: From October 1993 through April 1996, a total number of 52 cancer patients was enrolled in the study. The tumor sites in these patients were: breast (n = 41), lung (n = 4), head and neck (n = 3) as well as prostate, bladder, rectal cancer and Hodgkin' …
PATIENTS AND METHODS: From October 1993 through April 1996, a total number of 52 cancer patients was enrolled in the study. The tumor sites …