miércoles, 23 de marzo de 2016

Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing | Orphanet Journal of Rare Diseases | Full Text

Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing | Orphanet Journal of Rare Diseases | Full Text

Orphanet Journal of Rare Diseases - IMPACT FACTOR 3.358

The following new article has just been published in Orphanet Journal of Rare Diseases



Research  

Calmels N, Greff G, Obringer C, Kempf N, Gasnier C, Tarabeux J, Miguet M, Baujat G, Bessis D, Bretones P, Cavau A, Digeon B, Doco-Fenzy M, Doray B, Feillet F, Gardeazabal J, Gener B, Julia S, Llano-Rivas I, Mazur A, Michot C, Renaldo-Robin F, Rossi M, Sabouraud P, Keren B, Depienne C, Muller J, Mandel J, Laugel V

Orphanet Journal of Rare Diseases 2016, 11 :26 (22 March 2016)

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