Best matches for Bayraklı F[Author]:

Hereditary spastic paraplegia with recessive trait caused by mutation in KLC4 gene. Bayrakli F et al. J Hum Genet. (2015)

Mutation in MEOX1 gene causes a recessive Klippel-Feil syndrome subtype. Bayrakli F et al. BMC Genet. (2013)

Neural tube defect family with recessive trait linked to chromosome 9q21.12-21.31. Bayri Y et al. Childs Nerv Syst. (2015)

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