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Results 1 to 25 of 43948

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

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

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

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

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

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

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

Prenatal diagnosis of chromosomal imbalancesWELLESLEY, Diana G; LUCASSEN, Anneke.Archives of disease in childhood. Fetal and neonatal edition. 2014, Vol 99, Num 4, issn 1359-2998, F338-F341Article

Chromosomal aberrations involving telomeres and interstitial telomeric sequencesBOLZAN, Alejandro D.Mutagenesis. 2012, Vol 27, Num 1, pp 1-15, issn 0267-8357, 15 p.Article

Understanding aneuploidySIEGEL, Dawn H; SYBERT, Virginia P.Pediatric dermatology. 2005, Vol 22, Num 3, pp 270-275, issn 0736-8046, 6 p.Article

Investigations into the concept of a threshold for topoisomerase inhibitor-induced clastogenicityLYNCH, Anthony; HARVEY, James; AYLOTT, Michael et al.Mutagenesis. 2003, Vol 18, Num 4, pp 345-353, issn 0267-8357, 9 p.Article

Chromosomal aberrations: formation, identification and distributionOBE, G; PFEIFFER, P; SAVAGE, J. R. K et al.Mutation research. Fundamental and molecular mechanisms of mutagenesis. 2002, Vol 504, Num 1-2, pp 17-36, issn 1386-1964Conference Paper

Colloque de l'Association des Cytogénéticiens de Langue Française 1999Annales de génétique (Paris). 1999, Vol 42, Num 4, pp 247-256, issn 0003-3995Conference Proceedings

Chromosomal aberrations defining uveal melanoma of poor prognosisPRESCHER, G; BORNFELD, N; HORSTHEMKE, B et al.Lancet (British edition). 1992, Vol 339, Num 8794, pp 691-692, issn 0140-6736Article

Turner syndrome as a candidate pseudoautosomal disorderNUSBAUM, N. J.Medical hypotheses. 1992, Vol 39, Num 2, pp 156-158, issn 0306-9877Article

Frecuencia de mixoploidias en 85 casos indice con sindrome de Down = Frequency of mixodiploidy in 85 patients with Down's syndromeARMENDARES, S; BUENTELLOS, L; SALAMANCA, F et al.Revista de investigacion clinica. 1990, Vol 42, Num 2, pp 103-108, issn 0034-8376, 6 p.Article

Karyotype/phenotype controversy : genetic and molecular implications of alternative hypothesesWILSON, G. N.American journal of medical genetics. 1990, Vol 36, Num 4, pp 500-505, issn 0148-7299Article

Mutations in CEP57 cause mosaic variegated aneuploidy syndromeSNAPE, Katie; HANKS, Sandra; CLAYTON-SMITH, Jill et al.Nature genetics. 2011, Vol 43, Num 6, pp 527-529, issn 1061-4036, 3 p.Article

A clinical and molecular study of 26 females with Xp deletions with special emphasis on inherited deletionsLACHLAN, K. L; YOUINGS, S; COSTA, T et al.Human genetics. 2006, Vol 118, Num 5, pp 640-651, issn 0340-6717, 12 p.Article

Aneuploidy-inducing capacity of two widely used pesticidesMATTIUZZO, Marta; FIORE, Mario; RICORDY, Ruggero et al.Carcinogenesis (New York. Print). 2006, Vol 27, Num 12, pp 2511-2518, issn 0143-3334, 8 p.Article

Chromosome abnormalities in referred patients ― a five year studyMITRA, A. B; MURTY, V. V. V. S; MAHENDRA PRATAP et al.Indian journal of medical research. 1985, Vol 87, pp 475-478, issn 0019-5340Article

A new microduplication syndrome encompassing the region of the Miller-Dieker (17p13 deletion) syndromeROOS, L; JONCH, A. E; KJAERGAARD, S et al.Journal of medical genetics. 2009, Vol 46, Num 10, pp 703-710, issn 0022-2593, 8 p.Article

Be Careful With Familial Unbalanced Chromosome Abnormalities!RODRIGUEZ, L; NIEBUHR, E; GARCIA, A et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 15, pp 2005-2007, issn 1552-4825, 3 p.Article

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