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Results 1-9 of 9 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2015
Genetic heritage of the balto-slavic speaking populations: a synthesis of autosomal, mitochondrial and Y-chromosomal data
Kushniarevich, A.
;
Utevska, O.
;
Chuhryaeva, M.
;
Agdzhoyan, A.
;
Dibirova, K.
;
Uktveryte, I.
;
Möls, M.
;
Mulahasanovic, L.
;
Pshenichnov, A.
;
Frolova, S.
;
Shanko, A.
;
Metspalu, E.
;
Reidla, M.
;
Tambets, K.
;
Tamm, E.
;
Koshel, S.
;
Zaporozhchenko, V.
;
Atramentova, L.
;
Kučinskas, V.
;
Davydenko, O.
;
et al.
;
Calafell, F.
2013
Y-Chromosome and mtDNA genetics reveal significant contrasts in affinities of modern Middle Eastern populations with European and African populations
Badro, D.
;
Douaihy, B.
;
Haber, M.
;
Youhanna, S.
;
Salloum, A.
;
Ghassibe-Sabbagh, M.
;
Johnsrud, B.
;
Khazen, G.
;
Matisoo-Smith, E.
;
Soria-Hernanz, D.
;
Wells, R.
;
Tyler-Smith, C.
;
Platt, D.
;
Zalloua, P.
;
Caramelli, D.
2009
Variation in Giardia: towards a taxonomic revision of the genus
Monis, P.
;
Caccio, S.
;
Thompson, R.
2015
Human-assisted invasions of Pacific islands by Litoria frogs: a case study of the bleating tree frog on Lord Howe Island
Plenderleith, T.
;
Smith, K.
;
Donnellan, S.
;
Reina, R.
;
Chapple, D.
;
Patterson, H.
2014
Mitochondrial genome sequencing in mesolithic North East Europe unearths a new sub-clade within the broadly distributed human haplogroup C1
Der Sarkissian, C.
;
Brotherton, P.
;
Balanovsky, O.
;
Templeton, J.
;
Llamas, B.
;
Soubrier, J.
;
Moiseyev, V.
;
Khartanovich, V.
;
Cooper, A.
;
Haak, W.
;
Genographic Consortium,
;
Achilli, A.
2014
AmericaPlex26: a SNaPshot multiplex system for genotyping the main human mitochondrial founder lineages of the Americas
Coutinho, A.
;
Valverde, G.
;
Fehren-Schmitz, L.
;
Cooper, A.
;
Barreto Romero, M.
;
Flores Espinoza, I.
;
Llamas, B.
;
Haak, W.
;
Achilli, A.
1997
Gene structure and subcellular localisation of FMR2, a member of a new family of putative transcription activators
Gecz, J.
;
Bielby, S.
;
Sutherland, G.
;
Mulley, J.
1998
The human dead ringer/bright homolog, DRIL1: cDNA cloning, gene structure, and mapping to D19S886, a marker on 19p13.3 that is strictly linked to the Peutz-Jeghers Syndrome.
Kortschak, R.
;
Reimann, H.
;
Zimmer, M.
;
Eyre, H.
;
Saint, R.
;
Jenne, D.
1997
Chromosomal localisation of the human P2y6 purinoceptor gene and phylogenetic analysis of the P2y purinoceptor family
Somers, G.
;
Hammet, F.
;
Woollatt, E.
;
Richards, R.
;
Southey, M.
;
Venter, D.
Discover
Author
2
Achilli, A.
2
Cooper, A.
2
Haak, W.
2
Llamas, B.
1
Agdzhoyan, A.
1
Atramentova, L.
1
Badro, D.
1
Balanovsky, O.
1
Barreto Romero, M.
1
Bielby, S.
.
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Subject
4
DNA, Mitochondrial
4
Molecular Sequence Data
3
Animals
3
Europe
3
Genographic Consortium
3
Haplotypes
3
Polymorphism, Single Nucleotide
2
Chromosome Mapping
2
Chromosomes, Human, Y
2
Cloning, Molecular
.
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Date issued
5
2010 - 2015
1
2000 - 2009
3
1997 - 1999