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Role of congenital hypertrophy of the retinal pigment epithelium in the predictive diagnosis of familial adenomatous polyposis.
Br J Surg. 1992 Jul;79(7):689-93. doi: 10.1002/bjs.1800790733.
Br J Surg. 1992.
PMID: 1322757
Prognostic value of monitoring a candidate immunophenotypic leukaemic stem/progenitor cell population in patients allografted for acute myeloid leukaemia.
Bradbury C, Houlton AE, Akiki S, Gregg R, Rindl M, Khan J, Ward J, Khan N, Griffiths M, Nagra S, Hills R, Burnett A, Russell N, Vyas P, Grimwade D, Craddock C, Freeman SD.
Bradbury C, et al. Among authors: rindl m.
Leukemia. 2015 Apr;29(4):988-91. doi: 10.1038/leu.2014.327. Epub 2014 Nov 26.
Leukemia. 2015.
PMID: 25425198
Free PMC article.
No abstract available.
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A trisomic germ cell line and precocious chromatid segregation leads to recurrent trisomy 21 conception.
Cozzi J, Conn CM, Harper J, Winston RM, Rindl M, Farndon PA, Delhanty JD.
Cozzi J, et al. Among authors: rindl m.
Hum Genet. 1999 Jan;104(1):23-8. doi: 10.1007/s004390050905.
Hum Genet. 1999.
PMID: 10071188
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Acquired isodisomy for chromosome 13 is common in AML, and associated with FLT3-itd mutations.
Griffiths M, Mason J, Rindl M, Akiki S, McMullan D, Stinton V, Powell H, Curtis A, Bown N, Craddock C.
Griffiths M, et al. Among authors: rindl m.
Leukemia. 2005 Dec;19(12):2355-8. doi: 10.1038/sj.leu.2403988.
Leukemia. 2005.
PMID: 16239911
No abstract available.
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