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Parental and chromosomal origin of unbalanced de novo structural chromosome abnormalities in manTHOMAS, N. Simon; DURKIE, Miranda; VAN ZYL, Berendine et al.Human genetics. 2006, Vol 119, Num 4, pp 444-450, issn 0340-6717, 7 p.Article

L'empreinte parentale = Parental imprintingJIRTLE, Randy; WEIDMAN, Jennifer.Pour la science. 2007, Num 362, pp 58-64, issn 0153-4092, 7 p.Article

Où l'on apprend que les génomes ont un sexe : Applications de l'épigénétique = Genomes have a sexCAVAILLE, Jérome.Biofutur (Puteaux). 2004, Vol 244, pp 32-35, issn 0294-3506, 4 p.Article

What good is genomic imprinting: The function of parent-specific gene expressionWILKINS, Jon F; HAIG, David.Nature reviews. Genetics (Print). 2003, Vol 4, Num 5, pp 359-368, issn 1471-0056, 10 p.Article

Parental origin and timing of de novo robertsonian translocation formationBANDYOPADHYAY, Ruma; HELLER, Anita; KNOX-DUBOIS, Cami et al.American journal of human genetics. 2002, Vol 71, Num 6, pp 1456-1462, issn 0002-9297, 7 p.Article

Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11FRANCKS, Clyde; DELISI, Lynn E; SHAW, Sarah H et al.Human molecular genetics (Print). 2003, Vol 12, Num 24, pp 3225-3230, issn 0964-6906, 6 p.Article

Metastable epialleles in mammalsRAKYAN, Vardhman K; BLEWITT, Marnie E; DRUKER, Riki et al.Trends in genetics (Regular ed.). 2002, Vol 18, Num 7, pp 348-351, issn 0168-9525Article

The Croatian scientific elite and its socio-professional rootsGOLUB, B.Scientometrics (Print). 1998, Vol 43, Num 2, pp 207-229, issn 0138-9130Article

SALL1 mutations in sporadic townes-brocks syndrome are of predominantly paternal origin without obvious paternal age effectBÖHM, Johann; MUNK-SCHULENBURG, Susanne; FELSCHER, Stephanie et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 18, pp 1904-1908, issn 1552-4825, 5 p.Article

Does thalidomide cause second generation birth defects?SMITHELLS, D.Drug safety. 1998, Vol 19, Num 5, pp 339-341, issn 0114-5916Article

Des aléas de la parentalité : Etre ou ne pas être parents = Some hazards of the parentality: to be or not to be parentsGOUBIER-BOULA, M.-O.International congress on cyberneticsCongrès international de cybernétique. 1998, pp 814-818, isbn 2-87215-004-8Conference Paper

Lack of parental origin specificity of altered alleles at 11p15 in testicular germ cell tumorsKRAGGERUD, Sigrid M; LEE, Maxwell P; SKOTHEIM, Rolf I et al.Cancer genetics and cytogenetics. 2003, Vol 147, Num 1, pp 1-8, issn 0165-4608, 8 p.Article

Elucidation of the minimal sequence required to imprint H19 transgenesCRANSTON, Melanie J; SPINKA, Tracy L; ELSON, David A et al.Genomics (San Diego, Calif.). 2001, Vol 73, Num 1, pp 98-107, issn 0888-7543Article

Human morbid genetics revisited: relevance of epigeneticsPETRONIS, Arturas.Trends in genetics (Regular ed.). 2001, Vol 17, Num 3, pp 142-146, issn 0168-9525Article

Forage yields of alfalfa populations derived from parents selected on the basis of molecular marker diversityKIDWELL, K. K; HARTWECK, L. M; YANDELL, B. S et al.Crop science. 1999, Vol 39, Num 1, pp 223-227, issn 0011-183XArticle

The mouse H19 locus mediates a transition between imprinted and non-imprinted DNA replication patternsGREALLY, J. M; STARR, D. J; HWANG, S et al.Human molecular genetics (Print). 1998, Vol 7, Num 1, pp 91-95, issn 0964-6906Article

Monoallelic expression and tissue specificity are associated with high crossover ratesNECSULEA, Anamaria; SEMON, Marie; DURET, Laurent et al.Trends in genetics (Regular ed.). 2009, Vol 25, Num 12, pp 519-522, issn 0168-9525, 4 p.Article

Parental origin of sequence variants associated with complex diseasesKONG, Augustine; STEINTHORSDOTTIR, Valgerdur; FRIGGE, Michael L et al.Nature (London). 2009, Vol 462, Num 7275, pp 868-874, issn 0028-0836, 7 p.Article

Asymétrie des génomes parentaux : Implications en pathologie = Differential epigenetic marking on imprinted genes and consequences in human diseasesHENCKEL, Amandine; FEIL, Robert.MS. Médecine sciences. 2008, Vol 24, Num 8-9, pp 747-752, issn 0767-0974, 6 p.Article

Inactivation du chromosome X et imprinting de l'Igf-2-R : un mécanisme comparable lié à des ARN non codants? = A common mechanism for X-chromosome inactivation and Igf-2-R imprinting?BLANCHET, J.-P.MS. Médecine sciences. 1998, Vol 14, Num 3, pp 344-347, issn 0767-0974Article

Sharing genetic origins information in donor assisted conception : Views from licensed centres on HFEA donor information form (91) 4BLYTH, E; HUNT, J.Human reproduction (Oxford. Print). 1998, Vol 13, Num 11, pp 3274-3277, issn 0268-1161Article

Improving seed yield in red clover through marker assisted parentage analysisVLEUGELS, Tim; CNOPS, Gerda; ROLDAN-RUIZ, Isabel et al.Euphytica. 2014, Vol 200, Num 2, pp 305-320, issn 0014-2336, 16 p.Article

Shift of spatial patterns during early recruitment in Fagus sylvatica: Evidence from seed dispersal estimates based on genotypic dataBONTEMPS, Aurore; KLEIN, Etienne K; ODDOU-MURATORIO, Sylvie et al.Forest ecology and management. 2013, Vol 305, pp 67-76, issn 0378-1127, 10 p.Article

Genetic Structure, Origins, and Relationships of Grapevine Cultivars from the Castilian Plateau of SpainSANTANA, José Carlos; HEUERTZ, Myriam; ARRANZ, César et al.American journal of enology and viticulture. 2010, Vol 61, Num 2, pp 214-224, issn 0002-9254, 11 p.Article

Parental origin of apparently balanced de novo complex chromosomal rearrangements investigated by microdissection, whole genome amplification, and microsatellite-mediated haplotype analysisGROSSMANN, V; HÖCKNER, M; FAUTH, C et al.Clinical genetics. 2010, Vol 78, Num 6, pp 548-553, issn 0009-9163, 6 p.Article

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