5516
Mohammed Mamdouh Sayed Ahmed
Clinical And Molecular Genetic Studies Of Specific Language Impairment
SLi, FOXP2 gene , D7S3052 mekw,

GATA repeat, Molecular Studies
Precise detection and accurate clinical diagnosis of specific language impairment among patients with language disorder to facilitate proper management and assess contribution of consanguinity in mode of inheritance. 2. To study the association of 2 markers residing in the vicinity of FOXP2 gene, namely; the repeat unit GATA of D7S3052 and the GATT tetranucleotide repeat in intron 6 of CFTR related to FOXP2 gene among children affected with specific language impairment. Identification of genes related to specific language impairment may facilitate future investigation of language development and its relation to human genome.
2016
M.D
Ain Shams
Medicine