Listar por autor "Pehlivan, Davut"
Mostrando ítems 1-3 de 3
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Copy-Number Variation Contributes to the Mutational Load of Bardet-Biedl Syndrome.
Lindstrand, Anna et al. | Fecha del documento: 2016 -
Recurrent CNVs and SNVs at the NPHP1 Locus Contribute Pathogenic Alleles to Bardet-Biedl Syndrome
Lindstrand, Anna et al. | Fecha del documento: 2014 -
Xq22 deletions and correlation with distinct neurological disease traits in females: Further evidence for a contiguous gene syndrome
Hijazi, Hadia et al. | Fecha del documento: 2020