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Results 1 to 25 of 382

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The matrilineal ancestry of Ashkenazi Jewry : Portrait of a recent founder eventBEHAR, Doron M; METSPALU, Ene; HERRNSTADT, Corinna et al.American journal of human genetics. 2006, Vol 78, Num 3, pp 487-497, issn 0002-9297, 11 p.Article

Founder mutations among the DutchZEEGERS, Maurice P. A; VAN POPPEL, Frans; VLIETINCK, Robert et al.European journal of human genetics. 2004, Vol 12, Num 7, pp 591-600, issn 1018-4813, 10 p.Article

Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east AsiansYAN, Denise; PARK, Hong-Joon; XUE ZHONG LIU et al.Human genetics. 2003, Vol 114, Num 1, pp 44-50, issn 0340-6717, 7 p.Article

Les théories de l'effet fondateur, Mayr, et la génétique des populations = Mayr and the founder principleTERZIAN, C; BIEMONT, C.Génétique sélection évolution. 1988, Vol 20, Num 1, pp 111-121, issn 0754-0264Article

A population-genetic test of founder effects and implications for Ashkenazi Jewish diseasesSLATKIN, Montgomery.American journal of human genetics. 2004, Vol 75, Num 2, pp 282-293, issn 0002-9297, 12 p.Article

Mutation history of the Roma/GypsiesMORAR, Bharti; GRESHAM, David; KALMAR, Lajos et al.American journal of human genetics. 2004, Vol 75, Num 4, pp 596-609, issn 0002-9297, 14 p.Article

On the effect of founder events on epistatic genetic varianceGOODNIGHT, C. J.Evolution. 1987, Vol 41, Num 1, pp 80-91, issn 0014-3820Article

L'effet fondateur : analyse expérimentale chez Drosophila melanogaster = The pounder effect: experimental analyses in D. mTERZIAN, Christophe; LEGAY, Jean-Marie.1986, 121 pThesis

The Genome-wide Patterns of Variation Expose Significant Substructure in a Founder PopulationJAKKULA, Eveliina; REHNSTROM, Karola; RIPATTI, Samuli et al.American journal of human genetics. 2008, Vol 83, Num 6, pp 787-794, issn 0002-9297, 8 p.Article

Y chromosome evidence for a founder effect in Ashkenazi JewsNEBEL, Almut; FILON, Dvora; FAERMAN, Marina et al.European journal of human genetics. 2005, Vol 13, Num 3, pp 388-391, issn 1018-4813, 4 p.Article

Founder effects and endangered speciesRYDER, O. A.Nature (London). 1988, Vol 331, Num 6155, issn 0028-0836, 396Article

Epistasis and the effect of founder events on the additive genetic varianceGOODNIGHT, C. J.Evolution. 1988, Vol 42, Num 3, pp 441-454, issn 0014-3820Article

Analysis of a scottish founder effect narrows the TAPVR-1 gene interval to chromosome 4q12BLEYL, Steven B; BOTTO, Lorenzo D; CAREY, John C et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 21, pp 2368-2373, issn 1552-4825, 6 p.Article

Change in the penetrance of founder BRCA1/2 mutations? A retrospective cohort studyFOULKES, W. D; BRUNET, J.-S; WONG, N et al.Journal of medical genetics. 2002, Vol 39, Num 6, pp 407-409, issn 0022-2593Article

Song similarity in an isolated population of fox sparrows (Passerella iliaca)NAUGLER, C. T; SMITH, P. C.The condor (Los Angeles, CA). 1991, Vol 93, Num 4, pp 1001-1003, issn 0010-5422Article

The probability of peak shifts in a founder populationROUHANI, S; BARTON, N. H.Journal of theoretical biology. 1987, Vol 126, Num 1, pp 51-62, issn 0022-5193Article

HOXB1 Founder Mutation in Humans Recapitulates the Phenotype of Hoxb1―/― MiceWEBB, Bryn D; SHAABAN, Sherin; OYSTRECK, Darren T et al.American journal of human genetics. 2012, Vol 91, Num 1, pp 171-179, issn 0002-9297, 9 p.Article

A population-specific HTR2B stop codon predisposes to severe impulsivityBEVILACQUA, Laura; DOLY, Stéphane; BELINER, Arnaud et al.Nature (London). 2010, Vol 468, Num 7327, pp 1061-1066, issn 0028-0836, 6 p.Article

Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophyLANDSVERK, Megan L; RUZZO, Elizabeth K; FARLOW, Martin R et al.Human molecular genetics (Print). 2009, Vol 18, Num 7, pp 1200-1208, issn 0964-6906, 9 p.Article

Population history and infrequent mutations : how old is a rare mutation? GUCY2D as a worked exampleHANEIN, Sylvain; PERRAULT, Isabelle; KAPLAN, Josseline et al.European journal of human genetics. 2008, Vol 16, Num 1, pp 115-123, issn 1018-4813, 9 p.Article

Multiple mutations responsible for frequent genetic diseases in isolated populationsZLOTOGORA, Joël.European journal of human genetics. 2007, Vol 15, Num 3, pp 272-278, issn 1018-4813, 7 p.Article

Megalencephalic leukoencephalopathy with subcortical cysts; a founder effect in Israeli patients and a higher than expected carrier rate among Libyan jewsBEN-ZEEV, Bruria; LEVY-NISSENBAUM, Etgar; FRYDMAN, Moshe et al.Human genetics. 2002, Vol 111, Num 2, pp 214-218, issn 0340-6717Article

Hereditary disorders among Iranian JewsZLOTOGORA, J.American journal of medical genetics. 1995, Vol 58, Num 1, pp 32-37, issn 0148-7299Article

Mitochondrial and nuclear genetic contribution of female founders to a contemporary population in Northeast QuebecHEYER, E.American journal of human genetics. 1995, Vol 56, Num 6, pp 1450-1455, issn 0002-9297Article

Transferrin variability and founder effect in Iceland reindeer, Rangifer tarandus LRØED, K. H; SOLDAL, A. V; THORISSON, S et al.Hereditas (Landskrona). 1985, Vol 103, Num 2, pp 161-164, issn 0018-0661Article

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