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Mutations in the interleukin receptor IL11RA cause autosomal recessive crouzon-like craniosynostosis
Keupp K.; Li Y.; Vargel I.; Hoischen A.; Richardson R.; Neveling K.; Wollnik B. (Wiley-Blackwell, 2013)We have characterized a novel autosomal recessive Crouzon-like craniosynostosis syndrome in a 12-affected member family from Antakya, Turkey, the presenting features of which include: multiple suture synostosis, midface ...