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pro vyhledávání: '"L L Cavalli-sforza"'
In 1951, the geneticist Luigi Luca Cavalli-Sforza was teaching in Parma when a student--a priest named Antonio Moroni--told him about rich church records of demography and marriages between relatives. After convincing the Church to open its records,
Autor:
M. Mazzoleni, G. Morganti, M. Boldrini, F. Sella, R. Ceppellini, A. Uggè, S. Cramarossa, L. L. Cavalli-Sforza, V. Formentano, G. Barigozzi, A. Buzzati-Traverso, L. Vajani, W. Molla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b8eb8b043c51dcc99c7f0075f278f57
https://doi.org/10.1159/000426164
https://doi.org/10.1159/000426164
Autor:
Bernard Jeune, L. L. Cavalli Sforza, C Calignano, Giuseppe Passarino, Jean-Marie Robine, G. De Benedictis, A Vallone, Claudio Franceschi, Anatoli I. Yashin
Publikováno v:
Passarino, G, Calignano, C, Vallone, A, Franceschi C.,, Jeune, B, Robine, J M, Yashin, A I, Cavalli Sforza, L L & De Benedictis, G 2002, ' Male/female ratio in centenarians : A possible role played by population genetic structure ', Experimental Gerontology, vol. 37, pp. 1283-1289 . https://doi.org/10.1016/s0531-5565(02)00140-7
All the demographic surveys on the centenarians have highlighted that females outnumber males. The centenarians' male/female (M/F) ratio reported by most studies ranges between 1:4 and 1:7. A puzzling 1:2 ratio was observed in Calabria, a Southern It
Autor:
K. Nayar, A Ruiz Linares, David Goldstein, Mark Seielstad, Joan M. Hebert, L. L. Cavalli Sforza, Marcus W. Feldman, A. A. Lin, Peter A. Underhill
Publikováno v:
Annals of Human Genetics. 60:401-408
Five polymorphic markers on the Y-chromosome (mostly microsatellites) were typed in 121 individuals from 13 populations around the world. With these markers 78 different haplotypes were detected. Haplotypes present more than once tend to be shared by
Autor:
L L, Cavalli-Sforza, M W, Feldman
Publikováno v:
Theoretical Population Biology. 37:3-25
Measures of variation in space are strongly affected by correlations between subdivisions used for sampling. Here we consider variation in gene frequencies across populations. Usually the variance of gene frequencies is standardized by dividing it by
Autor:
L. L. Cavalli Sforza, Giuseppe Passarino, Peter J. Oefner, J.B. Van Kirk, A. A. Lin, Peter A. Underhill, G. De Benedictis, Peidong Shen
Publikováno v:
Genomics. 71(1)
We have identified a dense set of markers useful in association studies involving the Werner syndrome (WRN) gene. The homozygotic disruption of the WRN gene is the cause of Werner disease. In addition, this gene is likely to be involved in many compl
Publikováno v:
Yi chuan xue bao = Acta genetica Sinica. 27(1)
The first set of geographic distribution maps of human gene in China are published, including 12 alleles: IB and IO of ABO system, m of MNS system, P1, Rh-D, A1 and A11 of HLA system, Gm1;21 and Gm1,3;5 of immunoglobulin, AK1, deficient type of G6PD,
Publikováno v:
Annals of human genetics. 64(Pt 2)
We genotyped 64 dinucleotide microsatellite repeats in individuals from populations that represent all inhabited continents. Microsatellite summary statistics are reported for these data, as well as for a data set that includes 28 out of 30 loci stud