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Results 1 to 25 of 20293

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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

The AZFc region of the Y chromosome features massive palindromes and uniform recurrent deletions in infertile menKURODA-KAWAGUCHI, Tomoko; SKALETSKY, Helen; PAGE, David C et al.Nature genetics. 2001, Vol 29, Num 3, pp 243-244, issn 1061-4036, 10 p.Article

Rôle de la translocation t(14;18)NADEL, Bertrand.Correspondances en onco-hématologie. 2014, Vol JUN, pp 4-9, issn 1954-4820, 6 p., HSArticle

A novel 2 bp deletion in the TM4SF2 gene is associated with MRX58ABIDI, F. E; HOLINSKI-FEDER, E; RITTINGER, O et al.Journal of medical genetics. 2002, Vol 39, Num 6, pp 430-433, issn 0022-2593Article

PGD for reciprocal translocationsDELHANTY, Joy D. A.Prenatal diagnosis. 2004, Vol 24, Num 7, issn 0197-3851, p. 552Article

A palindrome-mediated mechanism distinguishes translocations involving LCR-B of chromosome 22q11.2GETTER, Anthony L; SHAIKH, Tamim H; BUDARF, Marcia L et al.Human molecular genetics (Print). 2004, Vol 13, Num 1, pp 103-115, issn 0964-6906, 13 p.Article

BAC microarray analysis of 15q11-q13 rearrangements and the impact of segmental duplicationsLOCKE, D. P; SEGRAVES, R; NICHOLLS, R. D et al.Journal of medical genetics. 2004, Vol 41, Num 3, pp 175-182, issn 0022-2593, 8 p.Article

Overall DNA methylation and chromatin structure of normal and abnormal X chromosomesBERNARDINO-SGHERRI, J; FLAGIELLO, D; DUTRILLAUX, B et al.Cytogenetic and genome research. 2003, Vol 99, Num 1-4, pp 85-91, issn 1424-8581, 7 p.Article

Characterization of the slow-growth phenotype of S. cerevisiae whip/mgs1 sgs1 double deletion mutantsBRANZEI, Dana; SEKI, Masayuki; ONODA, Fumitoshi et al.DNA repair. 2002, Vol 1, Num 8, pp 671-682, issn 1568-7864Article

The presence of interstitial telomeric sequences in constitutional chromosome abnormalitiesMURTIF PARK, V; GUSTASHAW, K. M; WATHEN, T. M et al.American journal of human genetics. 1992, Vol 50, Num 5, pp 914-923, issn 0002-9297Article

Chromosomes in myelodysplastic syndrome: structural abnormalities of chromosome 11MUSILOVA, J; MICHALOVA, K; JAROSOVA, M et al.Annales de génétique (Paris). 1989, Vol 32, Num 1, pp 43-46, issn 0003-3995, 4 p.Article

Deletion (12) (q 15 q 21.2)WATSON, M. S; MCALLISTER-BARTON, L; MAHONEY, M. J et al.Journal of medical genetics. 1989, Vol 26, Num 5, pp 343-344, issn 0022-2593, 2 p.Article

Clinical consequences of deletion 1p35WENGER, S. L; STEELE, M. W; BECKER, D. J et al.Journal of medical genetics. 1988, Vol 25, Num 4, issn 0022-2593, 263Article

Interstitial deletion of the long arm of chromosome 4CHUDLEY, A. E; VERMA, M. R; RAY, M et al.American journal of medical genetics. 1988, Vol 31, Num 3, pp 549-551, issn 0148-7299Article

Les translocations chromosomiques: étude de 232 cas provenant de 144 familles = Chromosomal translocations: study of 232 carriers (from 144 families)GILLEROT, Y; KOULISCHER, L; JAUNIAUX, E et al.Journal de génétique humaine. 1988, Vol 36, Num 1-2, pp 45-57, issn 0021-7743Conference Paper

Translocations robertsoniennes et conseil génétique = Robertsonial translocations and genetic counsellingDE F. FORMIGA, L; LE MAREC, B; SERVILLE, F et al.Journal de génétique humaine. 1988, Vol 36, Num 1-2, pp 15-20, issn 0021-7743Conference Paper

Does ring syndrome exist? An analysis of 207 case reports on patients with a ring autosomeKOSZTOLANYI, G.Human genetics. 1987, Vol 75, Num 2, pp 174-179, issn 0340-6717Article

Analysis of a centric shift in the S11 chromosome of Aiolopus strepens (Orthoptera: Acrididae)SUJA, J. A; CAMACHO, J. P. M; CABRERO, J et al.Genetica ('s-Gravenhage). 1986, Vol 70, Num 3, pp 211-216, issn 0016-6707Article

Segregation and pairing of compound fifth-chromosomes in Lucilia cuprina malesFOSTER, G. G; MADDERN, R. H.Genetical research. 1985, Vol 46, Num 2, pp 149-167, issn 0016-6723Article

Molecular Pathways: Transcription Factories and Chromosomal TranslocationsOSBORNE, Cameron S.Clinical cancer research (Print). 2014, Vol 20, Num 2, pp 296-300, issn 1078-0432, 5 p.Article

Variegated Aneuploidy and Ring Chromosome Syndromes OverlapRIVERA, Horacio; DOMINGUEZ, María G.American journal of medical genetics. Part A. 2010, Vol 152, Num 1, pp 228-229, issn 1552-4825, 2 p.Article

Chromosomal translocations : revisited yet againROWLEY, Janet D.Blood. 2008, Vol 112, Num 6, pp 2183-2189, issn 0006-4971, 7 p.Article

Chromosomal Rearrangements Leading to MLL Gene Fusions : Clinical and Biological AspectsHARPER, David P; APIAN, Peter D.Cancer research (Chicago, Ill.). 2008, Vol 68, Num 24, pp 10024-10027, issn 0008-5472, 4 p.Article

Switching on chromosomal translocationsRAMIRO, Almudena R; NUSSENZWEIG, Michel C; NUSSENZWEIG, André et al.Cancer research (Baltimore). 2006, Vol 66, Num 16, pp 7837-7839, issn 0008-5472, 3 p.Article

Molecular distinction between true centric fission and pericentric duplication-fissionPERRY, Jo; NOURI, Sara; PHUNG LA et al.Human genetics. 2005, Vol 116, Num 4, pp 300-310, issn 0340-6717, 11 p.Article

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