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pro vyhledávání: '"Louay H. Zayed"'
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 17, Iss 2, Pp 233-238 (2016)
Background and aim: Fraser syndrome (FS) is a rare autosomal recessive disorder characterized by cryptophthalmos, cutaneous syndactyly, laryngeal malformations and urogenital defects. It may be also associated with ear, nose and skeletal abnormalitie
Externí odkaz:
https://doaj.org/article/2a84cf70161d4cfbaffe178f957d391f