Deficiency of chromosome 8p21.1→4pter: case report and review of the literatureDOBYNS, W. B; DEWALD, G. W; CARLSON, R. O et al.American journal of medical genetics. 1985, Vol 22, Num 1, pp 125-134, issn 0148-7299Article

Constitutional and acquired trisomy 8SECKER-WALKER, L. M; FITCHETT, M.Leukemia research. 1995, Vol 19, Num 10, pp 737-740, issn 0145-2126Article

A case of chronic neutrophilic leukemia with trisomy 8ORAZI, A; CATTORETTI, G; SOZZI, G et al.Acta haematologica. 1989, Vol 81, Num 3, pp 148-151, issn 0001-5792Article

Haemophagocytosis in acute myeloid leukaemia t(8;16)HOWARD, Martin R; DICKINSON, Helen.British journal of haematology. 2007, Vol 137, Num 3, pp 180-180, issn 0007-1048, 1 p.Article

Deficiency of distal 8p - : report of two cases and review of the literaturePECILE, V; PETRONI, M. G; FERTZ, M. C et al.Clinical genetics. 1990, Vol 37, Num 4, pp 271-278, issn 0009-9163Article

Isochromosome (8p) in four patients with adenocarcinoma of the LungMIURA, I; RESAU, J; TOMIYASU, T et al.Cancer genetics and cytogenetics. 1990, Vol 48, Num 2, pp 203-207, issn 0165-4608, 5 p.Article

Familial syndrome with some features of the Langer-Giedion syndrome, and paracentric inversion of chromosome 8, inv 8(q11.23→q21.1)SHABTAI, F; SANDOWSKI, U; NISSIMOV, R et al.Clinical genetics. 1985, Vol 27, Num 6, pp 600-605, issn 0009-9163Article

PRMT1 interacts with AML1-ETO to promote its transcriptional activation and progenitor cell proliferative potentialSHIA, Wei-Jong; OKUMURA, Akiko J; ZHANG, Dong-Er et al.Blood. 2012, Vol 119, Num 21, pp 4953-4962, issn 0006-4971, 10 p.Article

Truncus arteriosus and duplication 8qDIGILIO, Maria Cristina; ANGIONI, Adriano; GIANNOTTI, Aldo et al.American journal of medical genetics. 2003, Vol 121A, Num 1, pp 79-81, issn 0148-7299, 3 p.Article

A recognisable behavioural phenotype associated with terminal deletions of the short arm of chromosome 8CLAEYS, I; HOLVOET, M; EYSKENS, B et al.American journal of medical genetics. 1997, Vol 74, Num 5, pp 515-520, issn 0148-7299Article

Persistence of AML1 rearrangement in peripheral blooc cells in t(8;21)KWONG, Y. L; WONG, K. F; CHAN, V et al.Cancer genetics and cytogenetics. 1996, Vol 88, Num 2, pp 151-154, issn 0165-4608Article

Familial translocation resulting in Wolf-Hirschhorn syndrome in two related unbalanced individuals : clinical evaluation of a 39-year-old man with Wolf-Hirschhorn syndromeWHEELER, P. G; WEAVER, D. D; PALMER, C. G et al.American journal of medical genetics. 1995, Vol 55, Num 4, pp 462-465, issn 0148-7299Article

Interstitial deletion of the short arm of chromosome 8: report of a patient and review of the literaturePLOMP, A. S; SCHRANDER-STUMPEL, C. T. R. M; ENGELEN, J. J. M et al.Genetic counseling. 1995, Vol 6, Num 1, pp 55-60, issn 1015-8146Article

Translocation (8;17)(p21;q21), a possible variant of t(15;17), in acute promyelocytic leukemiaMIURA, I; NISHINARI, T; HASHIMOTO, K et al.Cancer genetics and cytogenetics. 1994, Vol 72, Num 1, pp 75-77, issn 0165-4608Article

U-type exchange in a paracentric inversion as a possible mechanism of origin of an inverted tandem duplication of chromosome 8MITCHELL, J. J; VEKEMANS, M; LUSCOMBE, S et al.American journal of medical genetics. 1994, Vol 49, Num 4, pp 384-387, issn 0148-7299Article

Natural history of the recombinant (8) syndromeSUJANSKY, E; SMITH, A. C. M; PRESCOTT, K. E et al.American journal of medical genetics. 1993, Vol 47, Num 4, pp 512-525, issn 0148-7299Article

Jumping translocation involving band 3q13.3 in a case of acute monocytic leukemiaREIS, M. D; DUBE, I. D; PINKERTON, P. H et al.Cancer genetics and cytogenetics. 1991, Vol 51, Num 2, pp 189-194, issn 0165-4608Article

8;21 Translocation in acute nonlymphocytic leukemia: occurrence in M1 and M2 FAB subtypesDAVEY, D. D; PATIL, S. R; ECHTERNACHT, H et al.American journal of clinical pathology. 1989, Vol 92, Num 2, pp 172-176, issn 0002-9173Article

Translocation t(8;16) in acute monocytic leukemiaBECHER, R; HAAS, O. A; GRAEVEN, U et al.Cancer genetics and cytogenetics. 1988, Vol 34, Num 2, pp 265-271, issn 0165-4608Article

A final word on the tricho-rhinophalangeal syndromesBUHLER, E. M; BUHLER, U. K; BEUTLER, C et al.Clinical genetics. 1987, Vol 31, Num 4, pp 273-275, issn 0009-9163Article

Alternative involvement of two cytogenetically distinguishable breakpoints on chromosome 8 in Burkitt's lymphoma associated translocationsMANOLOV, G; MANOLVA, Y; KLEIN, G et al.Cancer genetics and cytogenetics. 1986, Vol 20, Num 1-2, pp 95-99, issn 0165-4608Article

Interstitial deletion of the long arm of chromosome 8 without Langer-Giedion syndromeKAZUKAWA, S; ENDO, M; FUJII, T et al.Japanese journal of psychiatry and neurology. 1986, Vol 40, Num 2, pp 221-226, issn 0912-2036Article

New variant translocation (1; 8; 21) in a case of acute myeloblastic leukemia (M2)TAGUCHI, H; KITAGAWA, T; YAMASHITA, M et al.Cancer genetics and cytogenetics. 1986, Vol 23, Num 3, pp 219-223, issn 0165-4608Article

The critical segment for the Langer-Giedion syndrome: 8q24.11→q24.12BOWEN, P; BIEDERMAN, B; HOO, J. J et al.Annales de génétique (Paris). 1985, Vol 28, Num 4, pp 224-227, issn 0003-3995Article

Acute mixed lineage leukemia with an inv(8)(p11q13) resulting in fusion of the genes for MOZ and TIF2JIAN LIANG; PROUTY, L; WILLIAMS, B. J et al.Blood. 1998, Vol 92, Num 6, pp 2118-2122, issn 0006-4971Article