KRAS gene mutations in Noonan syndrome familial cases cluster in the vicinity of the switch II region of the G-domain: report of another family with metopic craniosynostosis
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Craniosynostosis and Noonan syndrome with KRAS mutations: Expanding the phenotype with a case report and review of the literature.Craniosynostosis in patients with RASopathies: Accumulating clinical evidence for expanding the phenotype.Severe craniosynostosis with Noonan syndrome phenotype associated with SHOC2 mutation: clinical evidence of crosslink between FGFR and RAS signaling pathways
P2860
KRAS gene mutations in Noonan syndrome familial cases cluster in the vicinity of the switch II region of the G-domain: report of another family with metopic craniosynostosis
description
article
@en
im April 2012 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в травні 2012
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ലേഖനം
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name
KRAS gene mutations in Noonan ...... with metopic craniosynostosis
@en
KRAS gene mutations in Noonan ...... with metopic craniosynostosis
@nl
type
label
KRAS gene mutations in Noonan ...... with metopic craniosynostosis
@en
KRAS gene mutations in Noonan ...... with metopic craniosynostosis
@nl
prefLabel
KRAS gene mutations in Noonan ...... with metopic craniosynostosis
@en
KRAS gene mutations in Noonan ...... with metopic craniosynostosis
@nl
P2093
P2860
P50
P356
P1476
KRAS gene mutations in Noonan ...... with metopic craniosynostosis
@en
P2093
Alexandre C Pereira
Alexsandra C Malaquias
Amanda S Brasil
P2860
P304
P356
10.1002/AJMG.A.35270
P407
P577
2012-04-09T00:00:00Z