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1 Ergebnisse
1
Uncommon nucleotide excision repair phenotypes revealed by ..:
Calmels, Nadège
;
Greff, Géraldine
;
Obringer, Cathy
...
Orphanet Journal of Rare Diseases. 11 (2016) 1 - p. , 2016
Link:
https://doi.org/10.1186/s13023-016-0408-0
RT Journal T1
Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing
UL https://suche.suub.uni-bremen.de/peid=cr-10.1186_s13023-016-0408-0&Exemplar=1&LAN=DE A1 Calmels, Nadège A1 Greff, Géraldine A1 Obringer, Cathy A1 Kempf, Nadine A1 Gasnier, Claire A1 Tarabeux, Julien A1 Miguet, Marguerite A1 Baujat, Geneviève A1 Bessis, Didier A1 Bretones, Patricia A1 Cavau, Anne A1 Digeon, Béatrice A1 Doco-Fenzy, Martine A1 Doray, Bérénice A1 Feillet, François A1 Gardeazabal, Jesus A1 Gener, Blanca A1 Julia, Sophie A1 Llano-Rivas, Isabel A1 Mazur, Artur A1 Michot, Caroline A1 Renaldo-Robin, Florence A1 Rossi, Massimiliano A1 Sabouraud, Pascal A1 Keren, Boris A1 Depienne, Christel A1 Muller, Jean A1 Mandel, Jean-Louis A1 Laugel, Vincent PB Springer Science and Business Media LLC YR 2016 SN 1750-1172 JF Orphanet Journal of Rare Diseases VO 11 IS 1 LK http://dx.doi.org/https://doi.org/10.1186/s13023-016-0408-0 DO https://doi.org/10.1186/s13023-016-0408-0 SF ELIB - SuUB Bremen
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