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Compound heterozygosity for PTPN11 variants in a subject wi..:
Lorca, Rebeca
;
Pannone, Luca
;
Cuesta‐Llavona, Elías
...
Clinical Genetics. 99 (2021) 3 - p. 457-461 , 2021
Link:
https://doi.org/10.1111/cge.13904
RT Journal T1
Compound heterozygosity for PTPN11 variants in a subject with Noonan syndrome provides insights into the mechanism of SHP2‐related disorders
UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_cge.13904&Exemplar=1&LAN=DE A1 Lorca, Rebeca A1 Pannone, Luca A1 Cuesta‐Llavona, Elías A1 Bocchinfuso, Gianfranco A1 Rodríguez‐Reguero, Julian A1 Carpentieri, Giovanna A1 Hernando, Inés A1 Flex, Elisabetta A1 Tartaglia, Marco A1 Coto, Eliecer A1 Gómez, Juan A1 Martinelli, Simone PB Wiley YR 2021 SN 0009-9163 SN 1399-0004 JF Clinical Genetics VO 99 IS 3 SP 457 OP 461 LK http://dx.doi.org/https://doi.org/10.1111/cge.13904 DO https://doi.org/10.1111/cge.13904 SF ELIB - SuUB Bremen
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