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UnknownBrief Report of Variants Detected in Hereditary Hearing Loss Cases in Iran over a 3-Year Period.
Not available
S-EPMC6908923 | biostudies-literature
UnknownNovel CFTR Mutations in Two Iranian Families with Severe Cystic Fibrosis.
Not available
S-EPMC4983674 | biostudies-literature
UnknownChromosomal aberrations in pregnancy and fetal loss: Insight on the effect of consanguinity, review of 1625 cases.
Not available
S-EPMC6687859 | biostudies-literature
UnknownThe Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri Families.
Not available
S-EPMC4550366 | biostudies-literature
UnknownFirst Case of Macrocephaly, Dysmorphic Facies, and Psychomotor Retardation Harboring Co-inherited Variants in HERC1 and PMP22 Genes from Iran: Two Novel Variants.
Not available
S-EPMC11786211 | biostudies-literature
UnknownUnraveling the Genetic Landscape of Hearing Loss: A Comprehensive Study of Azeri Families in Ardabil, Iran.
Not available
S-EPMC11836346 | biostudies-literature
UnknownCharacterizing Genotypes and Phenotypes Associated with Dysfunction of Channel-Encoding Genes in a Cohort of Patients with Intellectual Disability.
Not available
S-EPMC10685845 | biostudies-literature
UnknownIdentifying the causes of recurrent pregnancy loss in consanguineous couples using whole exome sequencing on the products of miscarriage with no chromosomal abnormalities.
Not available
S-EPMC7997959 | biostudies-literature
UnknownBi-allelic loss of function variant in the NRCAM gene is associated with motor-predominant axonal polyneuropathy; the second report.
Not available
S-EPMC10094081 | biostudies-literature
UnknownClinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population.
Not available
S-EPMC10876633 | biostudies-literature
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