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Exome sequencing for diagnosis of congenital hemolytic anem..:
Mansour-Hendili, Lamisse
;
Aissat, Abdelrazak
;
Badaoui, Bouchra
...
Orphanet Journal of Rare Diseases. 15 (2020) 1 - p. , 2020
Link:
https://doi.org/10.1186/s13023-020-01425-5
RT Journal T1
Exome sequencing for diagnosis of congenital hemolytic anemia
UL https://suche.suub.uni-bremen.de/peid=cr-10.1186_s13023-020-01425-5&Exemplar=1&LAN=DE A1 Mansour-Hendili, Lamisse A1 Aissat, Abdelrazak A1 Badaoui, Bouchra A1 Sakka, Mehdi A1 Gameiro, Christine A1 Ortonne, Valérie A1 Wagner-Ballon, Orianne A1 Pissard, Serge A1 Picard, Véronique A1 Ghazal, Khaldoun A1 Bahuau, Michel A1 Guitton, Corinne A1 Mansour, Ziad A1 Duplan, Mylène A1 Petit, Arnaud A1 Costedoat-Chalumeau, Nathalie A1 Michel, Marc A1 Bartolucci, Pablo A1 Moutereau, Stéphane A1 Funalot, Benoît A1 Galactéros, Frédéric PB Springer Science and Business Media LLC YR 2020 SN 1750-1172 JF Orphanet Journal of Rare Diseases VO 15 IS 1 LK http://dx.doi.org/https://doi.org/10.1186/s13023-020-01425-5 DO https://doi.org/10.1186/s13023-020-01425-5 SF ELIB - SuUB Bremen
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