Pascal and Francis Bibliographic Databases

Help

Search results

Your search

kw.\*:("Chromosomal aberration")

Filter

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Document Type [dt]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Publication Year[py]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Discipline (document) [di]

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Language

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Author Country

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Origin

A-Z Z-A Frequency ↓ Frequency ↑
Export in CSV

Results 1 to 25 of 52024

  • Page / 2081

Export

Selection :

  • and

In vitro and in vivo chromosomal aberrations induced by megazolNESSLANY, Fabrice; BRUGIER, Serge; MOURIES, Marie-Annick et al.Mutation research. Genetic toxicology and environmental mutagenesis. 2004, Vol 560, Num 2, pp 147-158, issn 1383-5718, 12 p.Article

Dossier sur les trisomiques 21Réadaptation (Paris). 1995, Num 416, issn 0484-0305, Pagination mult.[48 p.]Serial Issue

Chromosomal abnormalities in leukemiaCORK, A.The American journal of medical technology. 1983, Vol 49, Num 10, pp 703-714, issn 0002-9335Article

Anomalies chromosomiques et myélofibroses = Abnormal chromosomes and myelosclerosesBERGER, R.Actualités hématologiques. 1983, Vol 17, pp 97-102, issn 0567-8757Article

CHROMOSOMAL ABNORMALITIES OF A MEDIASTINAL EMBRYONAL CELL CARCINOMA IN A PATIENT WITH 47, XXY KLINEFELTER SYNDROME: EVIDENCE FOR THE PREMEIOTIC ORIGIN OF A GERM CELL TUMOR = ANOMALIES CHROMOSOMIQUES DU CANCER A CELLULES EMBRYONNAIRES MEDIASTINALES CHEZ UN MALADE ATTEINT D'UN SYNDROME DE KLINEFELTER A 47 XXY: MISE EN EVIDENCE D'UNE ORIGINE PREMEIOTIQUE DE LA TUMEUR A CELLULES GERMINALESMANN BD; SPARKES RS; KERN DH et al.1983; CANCER GENETICS AND CYTOGENETICS; ISSN 0165-4608; NLD; DA. 1983; VOL. 8; NO 3; PP. 191-196; ABS. ENG; BIBL. 20 REF.; FIGArticle

Nonrandom chromosome alterations in rhabdomyosarcomaTRENT, J; CASPER, J; MELTZER, P et al.Cancer genetics and cytogenetics. 1985, Vol 16, Num 3, pp 189-197, issn 0165-4608Article

Chromosome studies in polycythemia vera patients = Etudes des chromosomes dans la polycythémie vraieBERGER, R; BERNHEIM, A; LE CONIAT, M et al.Cancer genetics and cytogenetics. 1984, Vol 12, Num 3, pp 217-223, issn 0165-4608Article

Prognostic implications of in vitro colony studies and clonal chromosomal aberrations in adults with acute leukaemiaHÖRNSTED, P; LINDQVIST, R; GAHRTON, G et al.Scandinavian journal of haematology. 1984, Vol 32, Num 3, pp 297-305, issn 0036-553XArticle

Chromosome abnormalities in chronic myeloid leukemi in childrenPUCHKOWA, G. P; PRIGOGINA, E. L; FLEISCHMANN, E. W et al.Human genetics. 1983, Vol 64, Num 3, pp 257-262, issn 0340-6717Article

Translocation heterozygosity in Phlox drummondii HookSRIVASTAV, P. K; RAMA RAO, S; RAINA, S. N et al.1983, Vol 26, Num 2, pp 131-134Article

Novel reciprocal translocation between chromosomes and 9 found in a patient with myeloproliferative disorder = Nouvelle translocation réciproque entre les chromosomes 8 et 9 chez un malade atteint d'affection myéloproliférativeFRIEDHOFF, F; RAJENDRA, B; MOODY, R et al.Cancer genetics and cytogenetics. 1983, Vol 9, Num 4, pp 391-394, issn 0165-4608Article

Impact of medical genetics on environmental medicineBECKMAN, L.Clinical genetics. 1989, Vol 36, Num 5, pp 348-356, issn 0009-9163, 9 p.Conference Paper

Chromosomal mosaicism confined to the placenta in human conceptionsKALOUSEK, D. K; DILL, F. J.Science (Washington, D.C.). 1983, Vol 221, Num 4611, pp 665-667, issn 0036-8075Article

Significance of chromosome change to hematopoietic neoplasms = Signification des modifications chromosomiques des hémopathies malignesCHAGANTI, R. S. K.Blood. 1983, Vol 62, Num 3, pp 515-524, issn 0006-4971Article

Cytogenetic effects of hexavalent chromium in Bulgarian chromium platersBENOVA, Donka; HADJIDEKOVA, Valeria; NATARAJAN, Adayapalam T et al.Mutation research. Genetic toxicology and environmental mutagenesis. 2002, Vol 514, Num 1-2, pp 29-38, issn 1383-5718Article

Cytogenetic study in multiple myeloma = Etude cytogénétique dans le myélome multipleFERTI, A; PANAMI, A; ARAPAKIS, G et al.Cancer genetics and cytogenetics. 1984, Vol 12, Num 3, pp 247-253, issn 0165-4608Article

8;21 translocution in acute granulocytic leukaemia: cytological, cytochemical and clinical features = Translocation 8;21 dans la leucémie granulocytaire aiguë: aspects cytologiques, cytochimiques et cliniquesSWIRSKY, D. M; LI, Y. S; MATTHEWS, J. G et al.British journal of haematology. 1984, Vol 56, Num 2, pp 199-213, issn 0007-1048Article

Cytogenetic studies in spontaneous abortusesANDREWS, T; DUNLOP, W; ROBERTS, D. F et al.Human genetics. 1984, Vol 66, Num 1, pp 77-84, issn 0340-6717Article

Association of an inversion of chromosome 16 with abnormal marrow eosinophils in acute myelomonocytic leukemia. A unique cytogenetic-clinicopathological associationLE BEAU, M. M; LARSON, R. A; BITTER, M. A et al.The New England journal of medicine. 1983, Vol 309, Num 11, pp 630-636, issn 0028-4793Article

Chromosome aberrations: past, present and futureNATARAJAN, A. T.Mutation research. Fundamental and molecular mechanisms of mutagenesis. 2002, Vol 504, Num 1-2, pp 3-16, issn 1386-1964Conference Paper

Intrachanges as part of complex chromosome-type exchange aberrationsBOEI, J. J. W. A; VERMEULEN, S; MOSER, J et al.Mutation research. Fundamental and molecular mechanisms of mutagenesis. 2002, Vol 504, Num 1-2, pp 47-55, issn 1386-1964Conference Paper

Importance of detecting numerical versus structural chromosome aberrationsKIRSCH-VOLDERS, Micheline; VANHAUWAERT, Annelies; DE BOECK, Marlies et al.Mutation research. Fundamental and molecular mechanisms of mutagenesis. 2002, Vol 504, Num 1-2, pp 137-148, issn 1386-1964Conference Paper

Chromosomes and neoplasiaSANGER, W. G.Annals of clinical and laboratory science. 1983, Vol 13, Num 5, pp 366-370, issn 0091-7370Article

Acquired idiopathic sideroblastic anemia: A new chromosomal abnormalitySCHULMAN, P; KARDON, N; WEINER, R et al.Cancer genetics and cytogenetics. 1983, Vol 9, Num 4, pp 341-345, issn 0165-4608Article

Anomalies chromosomiques chez l'homme stérile: étude de 321 sujets = Chromatic anomalies in sterile men: 321 casesROUSSET, H; PASTEUR, X; BERTHEAS, M. F et al.La Presse médicale (1983). 1983, Vol 12, Num 47, issn 0755-4982, 3007Article

  • Page / 2081