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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

RESULTS OF 538 CHROMOSOME STUDIES ON PATIENTS REFERRED FOR CYTOGENETIC ANALYSIS = RESULTATS DE 538 ETUDES CHROMOSOMIQUES CHEZ DES PATIENTS ADRESSES POUR ANALYSE CYTOGENETIQUEMULCAHY MT; JENKYN J.1972; MED. J. AUSTRAL.; AUSTRAL.; DA. 1972; VOL. 2; NO 24; PP. 1333-1338; BIBL. 13REF.Serial Issue

HUMAN POPULATION CYTOGENETICSJACOBS PA.1973; EXCERPTA MED., INTERNATION. CONGR. SER.,; PAYS-BAS; DA. 1973; NO 250; PP. 232-242; BIBL. 18REF.; (C.R. IVECONGR. INT. GENET. HUM.; PARIS; 1971)Conference Paper

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

DIAGNOSIS OF DOWN'S SYNDROME: CLINICAL VS. LABORATORY = DIAGNOSTIC DU SYNDROME DE DOWN: CLINIQUE CONTRE LABORATOIRE1972; CLIN. PEDIATR.; U.S.A.; DA. 1972; VOL. 11; NO 6; PP. 353-356; BIBL. 4 REF.Serial Issue

LES ANOMALIES CONGENITALES DUES AUX ABERRATIONS CHROMOSOMIQUES1972; REV. FR. GYNECOL. OBSTETR.; FR.; DA. 1972; VOL. 67; NO 8-9; PP. 505-517Serial Issue

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

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

ANALYSE CYTOGENETIQUE DE L'AMPHIDIPLOIDE A 42 CHROMOSOMES SECALE SEGETALE X ACGILOPS TAMEZHLUMOV FK.1975; CITOL. I GENET., U.S.S.R.; S.S.S.R.; DA. 1975; VOL. 9; NO 4; PP. 338-342; ABS. ANGL.; BIBL. 33 REF.Article