Approche moléculaire des remaniements du chromosome 22 humain observés dans des pathologies tumorales non hématologiques: cas particulier de la t(11; 22) du Sarcome = Molecular approach of human chromosome 22 rearrangements observed in non hematologic tumoral pathologies with particular interest to the t(11; 22) Ewing's sarcoma specific translocationDelattre, Olivier; Thomas, Gilles.1991, 117 p.Thesis

A first-generation linkage disequilibrium map of human chromosome 22DAWSON, Elisabeth; ABECASIS, Goncalo R; CARTER, David et al.Nature (London). 2002, Vol 418, Num 6897, pp 544-548, issn 0028-0836Article

The molecular genetics of the 22q11-associated schizophreniaKARAYIORGOU, Maria; GOGOS, Joseph A.Molecular brain research. 2004, Vol 132, Num 2, pp 95-104, issn 0169-328X, 10 p.Conference Paper

Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locusSCAMBLER, P. J; KELLY, D; LINDSAY, E et al.Lancet (British edition). 1992, Vol 339, Num 8802, pp 1138-1139, issn 0140-6736Article

Polymorphic bovine microsatellites INRAMTT178, INRAMTT180 and INRAMTT183VELMALA, R; BAIMAN, D; VIRTA, A et al.Animal genetics (Print). 1995, Vol 26, Num 3, pp 209-210, issn 0268-9146Article

MLC1 gene is associated with schizophrenia and bipolar disorder in southern indiaVERMA, Ranjana; MUKERJI, Mitali; GROVER, Deepak et al.Biological psychiatry (1969). 2005, Vol 58, Num 1, pp 16-22, issn 0006-3223, 7 p.Article

Syndromes de délétion en 22q11 : fin d'enquête en vue ? = Syndromes associated with a 22q11 deletion : the end of the road ?LIPINSKI, M.MS. Médecine sciences. 1999, Vol 15, Num 8-9, pp 999-1002, issn 0767-0974Article

Does chromosome 22 have anything to do with sex determination: Further studies on a 46, XX, 22q11.2 del maleERICKSON, Robert P; SKINNER, Steve; JACQUET, Hélène et al.American journal of medical genetics. 2003, Vol 123A, Num 1, pp 64-67, issn 0148-7299, 4 p.Article

A Family-and Population-Based Study of the UFD1L Gene for SchizophreniaLIN XIE; LIN YE; JUN WEI et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2008, Vol 147, Num 7, pp 1076-1079, issn 1552-4841, 4 p.Article

A previously unrecognized microdeletion syndrome on chromosome 22 band qll.2 encompassing the BCR geneMIKLIAIL, Fady M; DESCARTES, Maria; PIOTROWSKI, Arkadiusz et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 18, pp 2178-2184, issn 1552-4825, 7 p.Article

A CASE OF TRISOMY 22 IN PONGO PYGMAEUSANDRLE M; FIEDLER W; RETT A et al.1979; CYTOGENET. CELL GENET.; CHE; DA. 1979; VOL. 24; NO 1; PP. 1-6; BIBL. 17 REF.Article

DNA pooling and dense marker maps : a systematic search for genes for cognitive abilityHILL, L; CRAIG, I. W; CHORNEY, K et al.Neuroreport (Oxford). 1999, Vol 10, Num 4, pp 843-848, issn 0959-4965Article

Six antimicrobial peptide genes of the cathelicidin family map to bovine chromosome 22q24 by fluorescence in situ hybridizationCASTIGLIONI, B; SCOCCHI, M; ZANETTI, M et al.Cytogenetics and cell genetics. 1996, Vol 75, Num 4, pp 240-242, issn 0301-0171Article

Three duplicons form a novel chimeric transcription unit in the pericentromeric region of chromosome 22q11BRIDGLAND, Lindsay; FOOTZ, Tim K; KARDEL, Melanie D et al.Human genetics. 2003, Vol 112, Num 1, pp 57-61, issn 0340-6717, 5 p.Article

Chromosome 22 : A model with implications for diagnostic imagingSTARSHAK, R. J.American journal of roentgenology (1976). 1996, Vol 167, Num 2, pp 315-324, issn 0361-803XArticle

Craniosynostosis : Another feature of the 22q11.2 deletion syndromeMCDONALD-MCGINN, Donna M; GRIPP, Karen W; BARTLETT, Scott P et al.American journal of medical genetics. 2005, Vol 136A, Num 4, pp 358-362, issn 0148-7299, 5 p.Article

Five new subjects with ring chromosome 22ISHMAEL, H. A; CATALDI, D; BEGLEITER, M. L et al.Clinical genetics. 2003, Vol 63, Num 5, pp 410-414, issn 0009-9163, 5 p.Article

Identification of limited regions of genetic aberrations in patients affected with Wilms' tumor using a tiling-path chromosome 22 arrayBENETKIEWICZ, Magdalena; DIAZ DE STAHL, Teresita; GÖRDÖR, Anita et al.International journal of cancer. 2006, Vol 119, Num 3, pp 571-578, issn 0020-7136, 8 p.Article

Involvement of a palindromic chromosome 22-specific low-copy repeat in a constitutional t(X; 22)(q27;q11)DEBEER, P; MOLS, R; HUYSMANS, C et al.Clinical genetics. 2002, Vol 62, Num 5, pp 410-414, issn 0009-9163, 5 p.Article

Interstitial loss and gain of sequences on chromosome 22 in meningiomas with normal karyotypePROWALD, Alexandra; WEMMERT, Silke; URBSCHAT, Steffi et al.International journal of oncology. 2005, Vol 26, Num 2, pp 385-393, issn 1019-6439, 9 p.Article

A 9.1-kb gap in the genome reference map is shown to be a stable deletion/insertion polymorphism of ancestral originROBLEDO, Renato; ORRU, Sandro; ROMANI, Massimo et al.Genomics (San Diego, Calif.). 2002, Vol 80, Num 6, pp 585-592, issn 0888-7543, 8 p.Article

Microdeletion and microduplication 22q11.2 screening in 295 patients with clinical features of digeorge/velocardiofacial syndromeBRUNET, Anna; GABAU, Elisabeth; PERICH, Rosa Maria et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 22, pp 2426-2432, issn 1552-4825, 7 p.Article

Loss of heterozygosity on chromosome 22q in gastrointestinal stromal tumors (GISTs) : a study on 50 casesLASOTA, Jerzy; WOZNIAK, Agnieszka; LIMON, Janusz et al.Laboratory investigation. 2005, Vol 85, Num 2, pp 237-247, issn 0023-6837, 11 p.Article

Separate and interacting effects within the catechol-O-methyltransferase (COMT) are associated with schizophreniaHANDOKO, H. Y; NYHOLT, D. R; MOWRY, B. J et al.Molecular psychiatry. 2005, Vol 10, Num 6, pp 589-597, issn 1359-4184, 9 p.Article

Evidence for Association of Bipolar Disorder to Haplotypes in the 22q12.3 Region Hear the Genes Stargazin, IFT27 and ParvalbuminNISSEN, Stephanie; LIANG, Sherri; SHEHKTMAN, Tatyana et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2012, Vol 159, Num 8, pp 941-950, issn 1552-4841, 10 p.Article