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Results 1 to 25 of 21058

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Detection of a 46,XX, der(3)t(3;4)(p25;p16.1) by using chromosome microdissectionGRAMMATICO, P; ROCCELLA, M; DE BERNARDO, C et al.Genetic counseling. 1998, Vol 9, Num 4, pp 259-264, issn 1015-8146Conference Paper

Identification of chromosome changes in acute myeloid leukemia (AML-M2) by molecular cytogeneticsLA STARZA, R; MATTEUCCI, C; CRESCENZI, B et al.Cancer genetics and cytogenetics. 1997, Vol 95, Num 2, pp 148-152, issn 0165-4608Article

Co-expression of two FAB-specific chromosome changes, t(15;17) and t(8;21), in a case of acute promyelocytic leukemiaMOVAFAGH, A; VARMA, N; VARMA, S et al.Annals of hematology (Print). 1996, Vol 72, Num 6, pp 375-378, issn 0939-5555, 3 p.Article

Clonal Genetic alterations in the lungs of current and former smokersMAO, L; JIN SOO LEE; KEMP, B. L et al.Journal of the National Cancer Institute. 1997, Vol 89, Num 12, pp 857-862, issn 0027-8874Article

Spindle-cell rhabdomyosarcoma with 2q36∼q37 involvementDEBIEC-RYCHTER, Maria; HAGEMEIJER, Anne; SCIOT, Raf et al.Cancer genetics and cytogenetics. 2003, Vol 140, Num 1, pp 62-65, issn 0165-4608, 4 p.Article

Allelic losses at 1p, 9q, 10q, 14q, and 22q in the progression of aggressive meningiomas and undifferentiated meningeal sarcomasLAMSZUS, K; KLUWE, L; MATSCHKE, J et al.Cancer genetics and cytogenetics. 1999, Vol 110, Num 2, pp 103-110, issn 0165-4608Article

A group of previously not recognized cytogenetic abnormalities in myeloid hematological malignanciesZHONG CHEN; RICHKIND, K; ROHERTY, S et al.Cancer genetics and cytogenetics. 1999, Vol 113, Num 2, pp 162-165, issn 0165-4608Article

Clinical and biologic implications of recurrent genomic aberrations in myelomaFONSECA, Rafael; BLOOD, Emily; BAILEY, Richard J et al.Blood. 2003, Vol 101, Num 11, pp 4569-4575, issn 0006-4971, 7 p.Article

Recurrent DNA copy number changes in 1q, 4q, 6q, 9p, 13q, 14q and 22q detected by comparative genomic hybridization in malignant mesotheliomaBJÖRKQVIST, A.-M; TAMMILEHTO, L; ANTTILA, S et al.British journal of cancer. 1997, Vol 75, Num 4, pp 523-527, issn 0007-0920Article

Allelic losses at chromosomes 1p, 2p, 6p, 10p, 13q, 17p, and 21q significantly correlate with the chromophobe subtype of renal cell carcinomaSCHWERDTLE, R. F; STÖRKEL, S; NEUHAUS, C et al.Cancer research (Baltimore). 1996, Vol 56, Num 13, pp 2927-2930, issn 0008-5472Article

The SUMO E3-ligase PIAS1 Regulates the Tumor Suppressor PML and Its Oncogenic Counterpart PML-RARARABELLINO, Andrea; CARTER, Brandon; PAOLO SCAGLIONI, Pier et al.Cancer research (Chicago, Ill.). 2012, Vol 72, Num 9, pp 2275-2284, issn 0008-5472, 10 p.Article

Chromatin modifications induced by PML-RARa repress critical targets in leukemogenesis as analyzed by ChIP-Chip. CommentaryPETTERSSON, Filippa; MILLER, Wilson H; AGRAWAL, Shuchi et al.Blood. 2008, Vol 111, Num 5, issn 0006-4971, 2498, 2887-2895 [10 p.]Article

The mobile nature of acrocentric elements illustrated by three unusual chromosome variantsREDDY, K. S; SULCOVA, V.Human genetics. 1998, Vol 102, Num 6, pp 653-662, issn 0340-6717Article

Translocation(8;20;21)(q22;q13;q22) in acute myeloblastic leukemia with maturation : A variant form of t(8;21)WONG, K. F; KWONG, Y. L; SO, C. C et al.Cancer genetics and cytogenetics. 1998, Vol 101, Num 1, pp 39-41, issn 0165-4608Article

Strikingly different molecular relapse kinetics in NPM1c, PML-RARA, RUNX1-RUNX1T1, and CBFB-MYH11 acute myeloid leukemiasOMMEN, Hans Beier; SCHNITTGER, Susanne; JOVANOVIC, Jelena V et al.Blood. 2010, Vol 115, Num 2, pp 198-205, issn 0006-4971, 8 p.Article

A new variant translocation of t(15;17) in a patient with acute promyelocytic leukemia (M3) : t(15;19;17)(q22;p13;q12)SAITOH, K; MIURA, I; MIURA, A. B et al.Cancer genetics and cytogenetics. 1998, Vol 102, Num 1, pp 15-18, issn 0165-4608Article

Translocation (6;9;22)(p25;q34;q11.2) identified by FISH in acute leukemiaGONZALEZ, G. J. R; NOTOHAMIPRODJO, M.Cancer genetics and cytogenetics. 1996, Vol 92, Num 1, pp 82-84, issn 0165-4608Article

Cytogenetic findings in reactive lymphoid hyperplasia: Significance of non-clonal t(3;14) and t(3;22)AU, Wing Y; HORSMAN, Douglas E; CONNORS, Joseph M et al.American journal of hematology. 2002, Vol 70, Num 2, pp 133-138, issn 0361-8609Article

Duplication 15q in a patient with t(8;21) acute myeloblastic leukemia (M2)LIJUN ZHANG; MULVIHILL, John J; KINASEWITZ, Gary T et al.Cancer genetics and cytogenetics. 2002, Vol 133, Num 2, pp 148-151, issn 0165-4608Article

Primary effusion lymphomas exhibit complex and recurrent cytogenetic abnormalitiesWILSON, Kathleen S; MCKENNA, Robert W; KROFT, Steven H et al.British journal of haematology. 2002, Vol 116, Num 1, pp 113-121, issn 0007-1048Article

Recombination in a balanced complex translocation of a mother leading to a balanced reciprocal translocation in the child. Review of 60 cases of balanced complex translocationsMADAN, K; NIEUWINT, A. W. M; VAN BEVER, Y et al.Human genetics. 1997, Vol 99, Num 6, pp 806-815, issn 0340-6717Article

Translocation (8;12;21)(q22.1;q24.1;q22.1) : A new masked type of t(8;21)(q22;q22) in a patient with acute myeloid leukemiaSAITOH, K; MIURA, I; SAITO, M et al.Cancer genetics and cytogenetics. 1997, Vol 96, Num 2, pp 111-114, issn 0165-4608Article

A new translocation, t(2;4;12)(p21;q12;p13), in CD7-positive acute myeloid leukemia : A variant form of t(4;12)HAMAGUCHI, H; NAGATA, K; YAMAMOTO, K et al.Cancer genetics and cytogenetics. 1999, Vol 114, Num 2, pp 96-99, issn 0165-4608Article

Cytogenetic and molecular characterization of a variant translocation associated with acute promyelocytic leukemia and involving chromosomes 11, 15 and 17CASULA, L; ARCHIDIACONO, N; GRAZIA PAU, M et al.Leukemia. 1996, Vol 10, Num 10, pp 1655-1657, issn 0887-6924Article

Variant t(1;15;17)(q23;q22;q23) in a case of acute promyelocytic leukemiaGALIENI, P; MAROTTA, G; VESSICHELLI, F et al.Leukemia. 1996, Vol 10, Num 10, pp 1658-1661, issn 0887-6924Article

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