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RING CHROMOSOME 15:R(15). IDENTIFICATION BY R BANDING. = CHROMOSOME EN ANNEAU 15:R(15). IDENTIFICATION PAR COLORATION EN BANDES RSTOLL C; JUIF JG; LUCKEL JC et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 27; NO 3; PP. 259-262; BIBL. 12 REF.Article

Assignment of the human P532 gene (HERC1) to chromosome 15q22 by fluorescence in situ hybridizationCRUZ, C; PALADUGU, A; VENTURA, F et al.Cytogenetics and cell genetics. 1999, Vol 86, Num 1, pp 68-69, issn 0301-0171Conference Paper

A potential rearrangement between CYP19 and TRPM7 genes on chromosome 15q21.2 as a cause of aromatase excess syndromeTIULPAKOV, Anatoly; KALINTCHENKO, Natalya; SEMITCHEVA, Tatyana et al.The Journal of clinical endocrinology and metabolism. 2005, Vol 90, Num 7, pp 4184-4190, issn 0021-972X, 7 p.Article

Genomewide linkage analysis in Costa Rican families implicates chromosome 15q14 as a candidate region for OCDROSS, Jessica; BADNER, Judith; SHAW MURRAY, Sarah et al.Human genetics. 2011, Vol 130, Num 6, pp 795-805, issn 0340-6717, 11 p.Article

ANALYSIS OF BANDING PATTERNS AND MOSAIC CONFIGURATIONS IN A CASE OF RING CHROMOSOME 15.SCHMID M; HENRICHS I; NESTLER H et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 41; NO 3; PP. 289-299; BIBL. 30 REF.Article

Distribution of the D15Z1 copy number polymorphismCOCKWELL, Annette E; JACOBS, Patricia A; CROLLA, John A et al.European journal of human genetics. 2007, Vol 15, Num 4, pp 441-445, issn 1018-4813, 5 p.Article

Assignment of human interleukin 16 (IL6) to chromosome 15q26.3 by radiation hybrid mappingKIM, H.-S.Cytogenetics and cell genetics. 1999, Vol 84, Num 1-2, issn 0301-0171, p. 93Article

RING CHROMOSOME 15 IN CHILD WITH A MINOR DYSMORPHISM OF PHENOTYPE.RUMENIE L; JOKSIMOVIC I; ANAF M et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 33; NO 2; PP. 187-188; BIBL. 5 REF.Article

RING CHROMOSOME 15 SYNDROMEFRYNS JP; TIMMERMANS J; D'HONDT F et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 51; NO 1; PP. 43-48; BIBL. 9 REF.Article

THE CHILD WITH CHROMOSOME RING 15WISNIEWSKI L; PRONICKA E; LECH H et al.1979; KLIN. PAEDIATR.; DEU; DA. 1979; VOL. 191; NO 4; PP. 429-432; ABS. GER; BIBL. 13 REF.Article

No evidence for DNA copy number change associated with the DUP25 cytogenetic phenotypeHOLLOX, Edward J; AL ARMOUR, John.European journal of human genetics. 2003, Vol 11, Num 12, pp 911-912, issn 1018-4813, 2 p.Article

Germline Mosacism in Shprintzen―Goldberg SyndromeSHANSKE, Alan L; GOODRICH, James T; ALA-KOKKO, Leena et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 7, pp 1574-1578, issn 1552-4825, 5 p.Article

Ring chromosome 15 : characterization by array CGHGLASS, Ian A; RAUEN, Katherine A; CHEN, Emily et al.Human genetics. 2006, Vol 118, Num 5, pp 611-617, issn 0340-6717, 7 p.Article

Association of deletions of the chromosomal region 15q24-ter and diaphragmatic hernia: A new case and discussion of the literatureHENGSTSCHLÄGER, Markus; MITTERMAYER, Christoph; REPA, Christa et al.Fetal diagnosis and therapy. 2004, Vol 19, Num 6, pp 510-512, issn 1015-3837, 3 p.Article

Assignment of an ionotropic glutamate receptor-like gene (GRINL1A) to human chromosome 15q22.1 by in situ hybridizationROGINSKI, R. S; MOHAN RAJ, B. K; FINKERNAGEL, S. W et al.Cytogenetics and cell genetics. 2001, Vol 93, Num 1-2, pp 143-144, issn 0301-0171Article

Delineation of a clinical syndrome caused by mosaic trisomy 15BÜHLER, E. M; BIENZ, G; STRAUMANN, E et al.American journal of medical genetics. 1996, Vol 62, Num 2, pp 109-112, issn 0148-7299Article

Mutation screening of the UBE3A/E6-AP gene in autistic disorderVEENSTRA-VANDERWEELE, J; GONEN, D; LEVENTHAL, B. L et al.Molecular psychiatry. 1999, Vol 4, Num 1, pp 64-67, issn 1359-4184Article

Assignement of the human mitochondrial NADP+ -specific isocitrate dehydrogenase (IDH2) gene to 15q26.1 by in situ hybridizationOH, I.-U; INAZAWA, J; KIM, Y.-O et al.Genomics (San Diego, Calif.). 1996, Vol 38, Num 1, pp 104-106, issn 0888-7543Article

Assignment of ISG20 encoding a new interferon-induced PML nuclear body-associated protein, to chromosome 15q26 by in situ hybridizationMATTEI, M.-G; TISSOT, C; GONGORA, C et al.Cytogenetics and cell genetics. 1997, Vol 79, Num 3-4, pp 286-287, issn 0301-0171Article

Radiation hybrid mapping of human ADAM10 gene to chromosome 15YAMAZAKI, K; MIZUI, Y; TANAKA, I et al.Genomics (San Diego, Calif.). 1997, Vol 45, Num 2, pp 457-459, issn 0888-7543Article

Assignment of the gene for ERC-55 (RCN2) to human chromosome band 15q22.33→q24.1 by in situ hybridizationWANG, J. Y; ZHEN, D. K; BIANCHI, D. W et al.Cytogenetics and cell genetics. 1997, Vol 79, Num 1-2, pp 60-61, issn 0301-0171Conference Paper

LA SINDROME R(15) (CROMOSOMA 15 AD ANELLO). DESCRIZIONE DI UN CASO. = LE SYNDROME R(15) (CHROMOSOME 15 EN ANNEAU). DESCRIPTION D'UN CASFERRANTE E; BOSCHERINI B; BRUNI L et al.1977; MINERVA PEDIATR.; ITAL.; DA. 1977; VOL. 29; NO 36; PP. 2163-2168; ABS. ANGL.; BIBL. 6 REF.Article

Refined localization of the human a-tropomyosin gene (TPM1) by genetic mappingMOGENSEN, J; KRUSE, T. A; BØRGLUM, A. D et al.Cytogenetics and cell genetics. 1999, Vol 84, Num 1-2, pp 35-36, issn 0301-0171Article

Assignment of the human dUTPase gene (DUT) to chromosome 15q15-q21.1 by fluorescence in situ hybridizationCOHEN, D; HENG, H. H. Q; SHI, X.-M et al.Genomics (San Diego, Calif.). 1997, Vol 40, Num 1, pp 213-215, issn 0888-7543Article

Assignmenta of the genes for cellular retinoic acid binding protein 1(CRABP1) and 2(CRABP2) to human chromosome band 15q24 and 1q21.3, respectively, by in situ hybridizationFLAGIELLO, D; APIOU, F; GIBAUD, A et al.Cytogenetics and cell genetics. 1997, Vol 76, Num 1-2, pp 17-18, issn 0301-0171Article

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