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Results 1 to 25 of 29466

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

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

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 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

Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletionSAITTA, Sulagna C; HARRIS, Stacy E; ASHLEY, Terry et al.Human molecular genetics (Print). 2004, Vol 13, Num 4, pp 417-428, issn 0964-6906, 12 p.Article

Nutritional supplementation with antioxidants decreases chromosomal damage in humansDUSINSKA, M; KAZIMIROVA, A; BARANCOKOVA, M et al.Mutagenesis. 2003, Vol 18, Num 4, pp 371-376, issn 0267-8357, 6 p.Article

Etude des aberrations chromosomiques induites par les rayons X au niveau des lymphocytes humainsDERRADJI, H; DZIRIL, M; AIT SAID, N et al.Louvain médical. 2003, Vol 122, Num 10, pp 353-357, issn 0024-6956, 5 p.Article

Anomalies chromosomiques équilibrées avec phénotype anormal = Balanced chromosomal rearrangements and abnormal phenotypeFRYNS, J.-P.Journal de génétique humaine. 1988, Vol 36, Num 1-2, pp 33-36, issn 0021-7743Conference Paper

Remaniements chromosomiques équilibrés à phénotype anormal = Balanced chromosomal rearrangements and abnormal phenotypePHILIP, N; MATTEI, M. G; PELLISSIER, M. C et al.Journal de génétique humaine. 1988, Vol 36, Num 1-2, pp 37-43, issn 0021-7743Conference Paper

A study of autism using X chromosome DNA probesCROWE, R. R; TSAI, L. Y; MURRAY, J. C et al.Biological psychiatry (1969). 1988, Vol 24, Num 4, pp 473-479, issn 0006-3223Article

Six weeks to twenty-one years old: a longitudinal study of children with Down's syndrome and their families (third Jack Tizard memorial lecture)CARR, J.Journal of child psychology and psychiatry and allied disciplines (Print). 1988, Vol 29, Num 4, pp 407-431, issn 0021-9630Article

Cytogenetic evaluation of 163 azoospermicsRIVAS, F; GARCIA-ESQUIVEL, L; DIAZ, M et al.Journal de génétique humaine. 1987, Vol 35, Num 4, pp 291-298, issn 0021-7743Article

Chromosomal aberrations in the lymphocytes of alcoholics and former alcoholicsMATSUSHIMA, Y.Neuropsychobiology. 1987, Vol 17, Num 1-2, pp 24-29, issn 0302-282XArticle

Flow cytometric scoring of micronucleated erythrocytes: an efficient platform for assessing in vivo cytogenetic damageDERTINGER, Stephen D; TOROUS, Dorothea K; HAYASHI, Makoto et al.Mutagenesis. 2011, Vol 26, Num 1, pp 139-145, issn 0267-8357, 7 p.Article

10qter Deletion : A New CasePICCIONE, Maria; ANTONA, Vincenzo; PIRO, Ettore et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 18, pp 2435-2438, issn 1552-4825, 4 p.Article

Cytogenetic damage in buccal epithelia and peripheral lymphocytes of young healthy individuals exposed to ozoneCHEN, Connie; ARJOMANDI, Mehrdad; HUAXIA QIN et al.Mutagenesis. 2006, Vol 21, Num 2, pp 131-137, issn 0267-8357, 7 p.Article

Double trisomySHIBO LI; HASSED, Susan; MULVIHILL, John J et al.American journal of medical genetics. 2004, Vol 124A, Num 1, pp 96-98, issn 0148-7299, 3 p.Article

Two direct repeats cause most human mtDNA deletionsSAMUELS, David C; SCHON, Eric A; CHINNERY, Patrick F et al.Trends in genetics (Regular ed.). 2004, Vol 20, Num 9, pp 393-398, issn 0168-9525, 6 p.Article

Deletion of Pten in mouse brain causes seizures, ataxia and defects in soma size resembling Lhermitte-Duclos diseaseBACKMAN, Stéphanie A; STAMBOLIC, Vuk; MAK, Tak W et al.Nature genetics. 2001, Vol 29, Num 4, pp 396-403, issn 1061-4036Article

Two methods for measuring the non-randomness of chromosome abnormalitiesDE BRAEKELEER, M; SMITH, B.Annals of human genetics. 1988, Vol 52, Num 1, pp 63-67, issn 0003-4800Article

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