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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

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

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

Les anomalies chromosomiques observées dans les leucoses myéloblastiques. A propos de deux observations = Chromosome abnormalities observed in acute myelocytic leukemia. 2 observationsGREGOIRE, M. J; GILGENKRANTZ, S; HUMBERT, J. C et al.Annales médicales de Nancy et de l'Est. 1983, Vol 22, pp 405-407, issn 0221-3796Article

Leucémie aiguë lymphoblastique de type Burkitt. Fréquence et aspects cytogénétiques = Burkitt type acute lymphoblastic leukemia. Frequency and genetic aspectsLAÏ, J. L; JOUET, J. P; ZAN DECKI, M et al.Nouvelle revue française d'hématologie. 1983, Vol 25, Num 5, pp 303-309, issn 0029-4810Article

Register of chromosomal abnormalities in QueenslandBELL, J. A; BOWLING, F. G; PEARN, J. H et al.Medical journal of Australia. 1983, Vol 2, Num 4, pp 186-189, issn 0025-729XArticle

Chromosome Breakage Is Regulated by the Interaction of the BLM Helicase and Topoisomerase IIαRUSSEL, Beatriz; BHATTACHARYYA, Saumitri; KEIRSEY, Jeremy et al.Cancer research (Chicago, Ill.). 2011, Vol 71, Num 2, pp 561-571, issn 0008-5472, 11 p.Article

Identification of the 21 monosomic lines in Avena byzantina C. Koch cv. KanotaMORIKAWA, T.Theoretical and Applied Genetics. 1985, Vol 70, Num 3, pp 271-278, issn 0040-5752Article

A new unusual translocation involving the short arms of chromosome 19 in Ph1-positive chronic myeloid leukemiaCAIMO, A; PARODI, C. M; RABATTI, C et al.Acta haematologica. 1984, Vol 71, Num 2, pp 124-127, issn 0001-5792Article

Cytogenetics and cancerWOLMAN, S. R.Archives of pathology & laboratory medicine (1976). 1984, Vol 108, Num 1, pp 15-19, issn 0363-0153Article

From chromosomes to molecular karyotyping : Small reciprocal insertion detected by spectral karyotyping (SKY) and delimited by array-CGH analysisMATTHAEI, Anja; WEMER, Walter; SCHROCK, Evelin et al.European journal of medical genetics. 2005, Vol 48, Num 3, pp 328-338, issn 1769-7212, 11 p.Article

Anticlastogenicity of chlorophyllin in the different cell cycle phases in cultured mammalian cellsNEGRAES, P. D; JORDAO, B. Q; VICENTINI, V. E. P et al.Mutation research. Genetic toxicology and environmental mutagenesis. 2004, Vol 557, Num 2, pp 177-182, issn 1383-5718, 6 p.Article

Association of deletions of the chromosomal region 15q24-ter and diaphragmatic hernia: A new case and discussion of the literatureHENGSTSCHLÄGER, Markus; MITTERMAYER, Christoph; REPA, Christa et al.Fetal diagnosis and therapy. 2004, Vol 19, Num 6, pp 510-512, issn 1015-3837, 3 p.Article

Chromosomal abnormality rates at amniocentesis and in live-born infantsHOOK, E. B; CROSS, P. K; SCHREINEMACHERS, D. M et al.JAMA, the journal of the American Medical Association. 1983, Vol 249, Num 15, pp 2034-2038, issn 0098-7484Article

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