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Refinement of the clinical and mutational spectrum ofUBE2Ad..:
Cordeddu, Viviana
;
Macke, Erica L.
;
Radio, Francesca Clementina
...
Clinical Genetics. 98 (2020) 2 - p. 172-178 , 2020
Link:
https://doi.org/10.1111/cge.13775
RT Journal T1
Refinement of the clinical and mutational spectrum ofUBE2Adeficiency syndrome
UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_cge.13775&Exemplar=1&LAN=DE A1 Cordeddu, Viviana A1 Macke, Erica L. A1 Radio, Francesca Clementina A1 Lo Cicero, Stefania A1 Pantaleoni, Francesca A1 Tatti, Massimo A1 Bellacchio, Emanuele A1 Ciolfi, Andrea A1 Agolini, Emanuele A1 Bruselles, Alessandro A1 Brunetti‐Pierri, Nicola A1 Suri, Mohnish A1 Josephs, Katherine S. A1 McEntagart, Meriel A1 Lanpher, Brendan A1 Nickels, Katherine C. A1 Haworth, Andrea A1 Reed, Laura A1 Cappuccio, Gerarda A1 Mammi, Isabella A1 Tarnowski, Jessica M. A1 Novelli, Antonio A1 Melis, Daniela A1 Callewaert, Bert A1 Dallapiccola, Bruno A1 Klee, Eric A1 Tartaglia, Marco A1 Deciphering Developmental Disorders Study PB Wiley YR 2020 SN 0009-9163 SN 1399-0004 JF Clinical Genetics VO 98 IS 2 SP 172 OP 178 LK http://dx.doi.org/https://doi.org/10.1111/cge.13775 DO https://doi.org/10.1111/cge.13775 SF ELIB - SuUB Bremen
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