权威例句
Marfan Syndrome type 5Mutation in fibrillin-1 and the Marfanoid-craniosynostosis (Shprintzen-Goldberg) syndrome.Mutations in ZDHHC9, Which Encodes a Palmitoyltransferase of NRAS and HRAS, Cause X-Linked Mental Retardation Associated with a Marf...Identification of FBN1 gene mutations in patients with ectopia lentis and marfanoid habitus.A form of X‐linked mental retardation with marfanoid habitusX-linked mental retardation with marfanoid habitus.The marfanoid hypermobility syndrome.Mutation screening of the fibrillin‐1 (FBN1) gene in 76 unrelated patients with Marfan syndrome or Marfanoid features leads to the ...Novel FBN1 mutations associated with predominant ectopia lentis and marfanoid habitus in Chinese patientsNew marfanoid syndrome with craniosynostosis
