Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 ( )
ALSMADI, Osama ; MEYER, Brian F ; ALKURAYA, Fowzan ; WAKIL, Salma ; ALKAYAL, Fadi ; AL-SAUD, Haya ; RAMZAN, Khushnooda ; AL-SAYED, Moeenaldeen
European journal of human genetics : EJHG, 2009-01, Vol.17 (1), p.14-21 [Periódico revisado por pares]Basingstoke: Nature Publishing Group
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