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

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

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

Prenatal diagnosis of mosaic tetrasomy 8pLE BRIS, Marie-Josée; MARCORELLES, Pascale; DE BRAEKELEER, Marc et al.American journal of medical genetics. 2003, Vol 120A, Num 1, pp 44-48, issn 0148-7299, 5 p.Article

Spontaneous regression of congenital leukaemia with an 8;16 translocationWEINTRAUB, Michael; KAPLINSKY, Chaim; AMARIGLIO, Ninette et al.British journal of haematology. 2000, Vol 111, Num 2, pp 641-643, issn 0007-1048Article

Ectopic NORs on human chromosomes 4qter and 8q11 : rare chromosomal variants detected in two familiesGUTTENBACH, M; HAAF, T; STEINLEIN, C et al.Journal of medical genetics. 1999, Vol 36, Num 4, pp 339-342, issn 0022-2593Article

Hypereosinophilic syndrome in a child mosaic for a congenital triplication of the short arm of chromosome 8EGESTEN, A; HÄGERSTRAND, I; KRISTOFFERSSON, U et al.British journal of haematology. 1997, Vol 96, Num 2, pp 369-373, issn 0007-1048Article

Distal 8p deletion (8) (p23.1) : An easily missed chromosomal abnormality that may be associated with congenital heart defect and mental retardationBAI-LIN WU; SCHNEIDER, G. H; SABATINO, D. E et al.American journal of medical genetics. 1996, Vol 62, Num 1, pp 77-83, issn 0148-7299Article

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

Mild phenotype associated with Inv Dup 8 (q21.2-q22.3) of maternal originTUPLER, R; PAGLIANO, E; BARBIERATO, L et al.American journal of medical genetics. 1996, Vol 62, Num 2, pp 160-163, issn 0148-7299Article

A specific chromosome aberration in a keratoacanthomaKIM, Dae-Kwang; KIM, Joo-Young; KIM, Hyeung-Tae et al.Cancer genetics and cytogenetics. 2003, Vol 142, Num 1, pp 70-72, issn 0165-4608, 3 p.Article

Fluorescence in situ hybridization analysis of masked (8;21)(q22;q22) translocationsHARRISON, C. J; RADFORD-WEISS, I; ROSS, F et al.Cancer genetics and cytogenetics. 1999, Vol 112, Num 1, pp 15-20, issn 0165-4608Conference Paper

Terminal detection in chromosome region 8p23.1-8pter in a child with features of velo-cardio-facial syndromeDEVRIENDT, K; DE MARS, K; DE COCK, P et al.Annales de génétique (Paris). 1995, Vol 38, Num 4, pp 228-230, issn 0003-3995Conference Paper

Blood consult: acute myeloid leukemia and the t(8;21)(q22;22)PARK, Jae H; HEDVAT, Cyrus V; TALLMAN, Martin S et al.Blood. 2011, Vol 117, Num 10, pp 2775-2777, issn 0006-4971, 3 p.Article

Structure of the AML1-ETO eTAFH domain-HEB peptide complex and its contribution to AML1-ETO activityPARK, Sangho; WEI CHEN; CIERPICKI, Tomasz et al.Blood. 2009, Vol 113, Num 15, pp 3558-3567, issn 0006-4971, 10 p.Article

Tetrasomy 8p: Discordance of amniotic fluid and blood karyotypesLOPEZ-PAJARES, I; DELICADO, A; LAPUNZINA, P et al.American journal of medical genetics. 2003, Vol 118A, Num 4, pp 353-357, issn 0148-7299, 5 p.Article

Hypereosinophilia associated with dysplastic features and a constitutional translocation previously not describedHERMIDA, Gerardo; MANJON, Raquel; RODRIGUEZ-SALAZAR, Marisa et al.Haematologica (Roma). 2000, Vol 85, Num 9, pp 997-998, issn 0390-6078Article

Familial transmission of a small supernumerary marker chromosome 8 identified by FISH : An updateROTHENMUND, H; CHUDLEY, A. E; DAWSON, A. J et al.American journal of medical genetics. 1997, Vol 72, Num 3, pp 339-342, issn 0148-7299Article

FRAXF in a patient with chromosome 8 duplicationVIANNA-MORGANTE, A. M; MINGRONI-NETTO, R. C; BARBOSA, A. C. C et al.Journal of medical genetics. 1996, Vol 33, Num 7, pp 611-614, issn 0022-2593Article

Aleukaemic acute myeloid leukaemia with t(8;21)(q22;q22)WONG, K. F; SIU, Lisa L. P; WONG, W. S et al.British journal of haematology. 2009, Vol 146, Num 4, issn 0007-1048, p. 345Article

Identification of AML1-ETO modulators by chemical genomicsCORSELLO, Steven M; ROTI, Giovanni; ROSS, Kenneth N et al.Blood. 2009, Vol 113, Num 24, pp 6193-6205, issn 0006-4971, 13 p.Article

T(8;16)(p11;p13) predisposes to a transient but potentially recurring neonatal leukemiaWONG, Kit-Fai; YUEN, Hui-Leung; SIU, Lisa L. P et al.Human pathology. 2008, Vol 39, Num 11, pp 1702-1707, issn 0046-8177, 6 p.Article

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