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Results 1 to 25 of 56

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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

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

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

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

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 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

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

COMTVal108/158Met Modifies mismatch negativity and cognitive function in 22q11 deletion syndromeBAKER, Kate; BALDEWEG, Torsten; SIVAGNANASUNDARAM, Sinthuja et al.Biological psychiatry (1969). 2005, Vol 58, Num 1, pp 23-31, issn 0006-3223, 9 p.Article

Investigation of the apolipoprotein-L (APOL) gene family and schizophrenia using a novel DNA pooling strategy for public database SNPsMCGHEE, Kevin A; MORRIS, Derek W; GILL, Michael et al.Schizophrenia research. 2005, Vol 76, Num 2-3, pp 231-238, issn 0920-9964, 8 p.Article

The breakpoint cluster region gene on chromosome 22q11 is associated with bipolar disorderHASHIMOTO, Ryota; OKADA, Takeya; KATO, Tadafumi et al.Biological psychiatry (1969). 2005, Vol 57, Num 10, pp 1097-1102, issn 0006-3223, 6 p.Article

Hypoparathyroidism in conotruncal heart defectsKOCH, Andreas; HOFBECK, Michael; BUHEITEL, Gernot et al.European journal of pediatrics. 2002, Vol 161, Num 4, pp 208-211, issn 0340-6199Article

A 21 years follow-up of a girl patient with a pseudodicentric bisatellited chromosome 22 associated with partial trisomy 22pter → 22ql2.1 : Clinical, cytogenetic and molecular observationsVAGLIO, Alicia; MILUNSKY, Aubrey; HUANG, Xin-Li et al.European journal of medical genetics. 2008, Vol 51, Num 4, pp 332-342, issn 1769-7212, 11 p.Article

Variant of the CHEK2 gene as a prognostic marker in glioblastoma multiforme. CommentarySIMON, Matthias; LUDWIG, Michael; BRUCE, Jeffrey N et al.Neurosurgery. 2006, Vol 59, Num 5, pp 1078-1085, issn 0148-396X, 8 p.Article

True hermaphroditism with 46,X, +22p/46,XY and gonadal mosaicism detected by fluorescence in situ hybridizationTAKANO, Takako; YAMANOUCHI, Yasuko; TANAKA, Fumihiko et al.Annales de génétique (Paris). 2003, Vol 46, Num 1, pp 57-60, issn 0003-3995, 4 p.Article

PRODH mutations and hyperprolinemia in a subset of schizophrenic patientsJACQUET, Hélène; RAUX, Grégory; BOU, Jacqueline et al.Human molecular genetics (Print). 2002, Vol 11, Num 19, pp 2243-2249, issn 0964-6906Article

Cellular myosin heavy chain in human leukocytes : isolation of 5' cDNA clones, characterization of the protein, chromosomal localization, and upregulation during meyloid differentiationTOOTHAKER, L. E; GONZALEZ, D. A; TUNG, N et al.Blood. 1991, Vol 78, Num 7, pp 1826-1833, issn 0006-4971Article

Mouse models of 22q11 deletion syndromePAYLOR, Richard; LINDSAY, Elizabeth.Biological psychiatry (1969). 2006, Vol 59, Num 12, pp 1172-1179, issn 0006-3223, 8 p.Article

No association found between 158 Val/Met polymorphism of the COMT gene and schizophrenia with minor physical anomaliesJOO, Eun-Jeong; JEONG, Seong-Hoon; AHN, Yong-Min et al.Psychiatry research. 2005, Vol 136, Num 2-3, pp 83-91, issn 0165-1781, 9 p.Article

Altered functioning of the cingulate gyrus in two cases of chromosome 22q11 deletion syndromeREIF, Andreas; FALLGATTER, Andreas J; EHLIS, Ann-Christine et al.Psychiatry research. Neuroimaging. 2004, Vol 132, Num 3, pp 273-278, issn 0925-4927, 6 p.Article

Arrangement of chromosome 11 and 22 territories, EWSR1 and FLI1 genes, and other genetic elements of these chromosomes in human lymphocytes and Ewing sarcoma cellsTASLEROVA, Renata; KOZUBEK, Stanislav; LUKASOVA, Emilie et al.Human genetics. 2003, Vol 112, Num 2, pp 143-155, issn 0340-6717, 13 p.Article

Comparative genomic hybridization in ganglioneuroblastomasAHTER DILSAD TORAMAN; KESER, Ibrahim; LÜLECI, Güven et al.Cancer genetics and cytogenetics. 2002, Vol 132, Num 1, pp 36-40, issn 0165-4608Article

Mutations of the INI1 rhabdoid tumor suppressor gene in medulloblastomas and primitive neuroectodermal tumors of the central nervous systemBIEGEL, J. A; FOGELGREN, B; ZHOU, J.-Y et al.Clinical cancer research. 2000, Vol 6, Num 7, pp 2759-2763, issn 1078-0432Article

Clinical manifestations of mutations in the neurofibromatosis type 2 gene in vestibular schwannomas (acoustic neuromas)WELLING, D. B.The Laryngoscope. 1998, Vol 108, Num 2, pp 178-189, issn 0023-852XConference Paper

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