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Biallelic variants in CENPF causing a phenotype distinct fr..:
Cappuccio, Gerarda
;
Brillante, Simona
;
Tammaro, Roberta
...
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 190 (2022) 1 - p. 102-108 , 2022
Link:
https://doi.org/10.1002/ajmg.c.31973
RT Journal T1 <Title>Biallelic variants in CENPF causing a phenotype distinct from Strømme syndrome</Title> UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_ajmg.c.31973&Exemplar=1&LAN=DE A1 Cappuccio, Gerarda A1 Brillante, Simona A1 Tammaro, Roberta A1 Pinelli, Michele A1 De Bernardi, Margherita Lucia A1 Gensini, Maria Grazia A1 Bijlsma, Emilia K. A1 Koopmann, Tamara T. A1 Hoffer, Mariette J. V. A1 McDonald, Kimberly A1 Hendon, Laura G. A1 Douzgou, Sofia A1 Deshpande, Charulata A1 D'Arrigo, Stefano A1 Torella, Annalaura A1 Nigro, Vincenzo A1 Franco, Brunella A1 Brunetti‐Pierri, Nicola PB Wiley YR 2022 SN 1552-4868 SN 1552-4876 JF American Journal of Medical Genetics Part C: Seminars in Medical Genetics VO 190 IS 1 SP 102 OP 108 LK http://dx.doi.org/https://doi.org/10.1002/ajmg.c.31973 DO https://doi.org/10.1002/ajmg.c.31973 SF ELIB - SuUB Bremen
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