Repository of Research and Investigative Information

Repository of Research and Investigative Information

Shoushtar Faculty of Medical Sciences

Items where Author is "Asl, J. M."

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Number of items: 5.


(2018) Identification of A Novel Missense Mutation in The Norrie Disease Gene: The First Molecular Genetic Analysis and Prenatal Diagnosis of Norrie Disease in An Iranian Family. Cell Journal. pp. 290-292. ISSN 2228-5806

(2018) Identification of Novel PTPRQ and MYO1A Mutations in An Iranian Pedigree with Autosomal Recessive Hearing Loss. Cell Journal. pp. 127-131. ISSN 2228-5806

(2018) Mutational spectrum of the CYP1B1 gene in Iranain primary congenital glaucoma family. Canadian Journal of Ophthalmology-Journal Canadien D Ophtalmologie. E87-E89. ISSN 0008-4182

(2017) Identification of a novel missence mutation in FGFR3 gene in an Iranian family with LADD syndrome by Next-Generation Sequencing. International Journal of Pediatric Otorhinolaryngology. pp. 192-196. ISSN 0165-5876

(2017) Next-generation sequencing identifies three novel missense variants in ILDR1 and MYO6 genes in an Iranian family with hearing loss with review of the literature. Int J Pediatr Otorhinolaryngol. pp. 103-108. ISSN 0165-5876

This list was generated on Thu Dec 1 00:49:15 2022 +0330.