Mutations in the interleukin receptor IL11RA cause autosomal recessive Crouzon-like craniosynostosis.
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Signaling pathways in osteogenesis and osteoclastogenesis: Lessons from cranial sutures and applications to regenerative medicine.Zebrafish Craniofacial Development: A Window into Early PatterningChromosome 1p31.1p31.3 Deletion in a Patient with Craniosynostosis, Central Nervous System and Renal Malformation: Case Report and Review of the LiteratureThe epidemiology of supernumerary teeth and the associated molecular mechanism.A biallelic mutation in IL6ST encoding the GP130 co-receptor causes immunodeficiency and craniosynostosis.Neurologic sequela in a patient with galactosemia potentially mediated by interleukin-11 dysfunction.Clinical genetics of craniosynostosis.Syndromes with supernumerary teeth.Novel 1q22-q23.1 duplication in a patient with lambdoid and metopic craniosynostosis, muscular hypotonia, and psychomotor retardation
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P2860
Mutations in the interleukin receptor IL11RA cause autosomal recessive Crouzon-like craniosynostosis.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 19 August 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Mutations in the interleukin r ...... Crouzon-like craniosynostosis.
@en
Mutations in the interleukin r ...... Crouzon-like craniosynostosis.
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type
label
Mutations in the interleukin r ...... Crouzon-like craniosynostosis.
@en
Mutations in the interleukin r ...... Crouzon-like craniosynostosis.
@nl
prefLabel
Mutations in the interleukin r ...... Crouzon-like craniosynostosis.
@en
Mutations in the interleukin r ...... Crouzon-like craniosynostosis.
@nl
P2093
P2860
P50
P356
P1476
Mutations in the interleukin r ...... Crouzon-like craniosynostosis.
@en
P2093
Bernd Wollnik
Burcu Akin
Christian Gilissen
Emin Mavili
Ersoy Konas
Gökhan Tunçbilek
Hartmut Collmann
Ibrahim Vargel
Joachim Grötzinger
P2860
P304
P356
10.1002/MGG3.28
P50
P577
2013-08-19T00:00:00Z