Repository of Research and Investigative Information
Shahid Sadoughi University of Medical Sciences
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(2017) B3GALNT2 mutations associated with non-syndromic autosomal recessive intellectual disability reveal a lack of genotype-phenotype associations in the muscular dystrophy-dystroglycanopathies. Genome medicine. p. 118. ISSN 1756-994X
(2013) Identification of Xq22.1-23 as a region linked with hereditary recurrent spontaneous abortion in a family. Iranian journal of reproductive medicine. pp. 659-64. ISSN 1680-6433