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A case of G1013R FBN1 mutation: A potential genotype–phenot..:
Willis, Brooke R.
;
Lee, Mianne
;
Rethanavelu, Kavitha
...
American Journal of Medical Genetics Part A. 182 (2020) 6 - p. 1329-1335 , 2020
Link:
https://doi.org/10.1002/ajmg.a.61567
RT Journal T1 <Title>A case of G1013R FBN1 mutation: A potential genotype–phenotype correlation in severe Marfan syndrome</Title> UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_ajmg.a.61567&Exemplar=1&LAN=DE A1 Willis, Brooke R. A1 Lee, Mianne A1 Rethanavelu, Kavitha A1 Fung, Jasmine L. F. A1 Wong, Rosanna M. S. A1 Hui, Peter A1 Yeung, Kit S. A1 Lo, Ivan F. M. A1 Chung, Brian H. Y. PB Wiley YR 2020 SN 1552-4825 SN 1552-4833 JF American Journal of Medical Genetics Part A VO 182 IS 6 SP 1329 OP 1335 LK http://dx.doi.org/https://doi.org/10.1002/ajmg.a.61567 DO https://doi.org/10.1002/ajmg.a.61567 SF ELIB - SuUB Bremen
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