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1
Novel MED12 variant in a multiplex Fragile X syndrome family: dual molecular etiology of two X-linked intellectual disabilities with autism in the same family
In: ISSN: 0301-4851 ; EISSN: 1573-4978 ; Molecular Biology Reports ; https://hal-riip.archives-ouvertes.fr/pasteur-03565723 ; Molecular Biology Reports, Springer Verlag, 2019, 46 (4), pp.4185 - 4193. ⟨10.1007/s11033-019-04869-6⟩ (2019)
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2
Spatially explicit analysis reveals complex human genetic gradients in the Iberian Peninsula
Pimenta, Joao; Lopes, Alexandra M.; Carracedo, Ange. - : Springer Nature, 2019
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3
Towards controlled terminology for reporting germline cancer susceptibility variants: an ENIGMA report.
Spurdle, Amanda B; Greville-Heygate, Stephanie; Antoniou, Antonis. - : BMJ, 2019. : J Med Genet, 2019
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4
European Roma groups show complex West Eurasian admixture footprints and a common South Asian genetic origin
Font-Porterias, N; Arauna, LR; Poveda, A. - : Public Library of Science, 2019
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5
Genome-wide diversity and demographic dynamics of Cameroon goats and their divergence from east African, north African, and Asian conspecifics
Tarekegn, Getinet Mekuriaw; Wouobeng, Patrick; Jaures, Kouam Simo. - : Public Library of Science, 2019
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