Found: 8
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Clinical presentation and natural history of infantile-onset ascending spastic paralysis from three families with an ALS2 founder variant.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Whole exome sequencing revealed a novel dystrophin-related protein-2 (DRP2) deletion in an Iranian family with symptoms of polyneuropathy.
- Published in:
- Iranian Journal of Basic Medical Sciences, 2019, v. 22, n. 5, p. 576, doi. 10.22038/ijbms.2019.30754.7414
- By:
- Publication type:
- Article
Coexistence of p190 BCR/ABL Transcript and CALR 52-bp Deletion in Chronic Myeloid Leukemia Blast Crisis: A Case Report.
- Published in:
- Mediterranean Journal of Hematology & Infectious Diseases, 2016, v. 8, p. 1, doi. 10.4084/MJHID.2016.002
- By:
- Publication type:
- Article
Rare cytogenetic abnormalities and alteration of microRNAs in acute myeloid leukemia and response to therapy.
- Published in:
- Oncology Reviews, 2015, v. 9, n. 1, p. 7, doi. 10.4081/oncol.2015.261
- By:
- Publication type:
- Article
Identification of A Novel Compound Heterozygous Mutation in BBS12 in An Iranian Family with Bardet-Biedl Syndrome Using Targeted Next Generation Sequencing.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Lipid Profile Improvement after Four Group Psychological Interventions in Combination to Nutritional and Physical Activity Instructing Among Overweight and Obese Individuals.
- Published in:
- Iranian Journal of Public Health, 2013, v. 42, n. 1, p. 86
- By:
- Publication type:
- Article
Identification of a novel truncating variant in AHI1 gene and a brief review on mutations spectrum.
- Published in:
- Molecular Biology Reports, 2021, v. 48, n. 6, p. 5339, doi. 10.1007/s11033-021-06508-5
- By:
- Publication type:
- Article
The Diagnostic Value of Gene Expression of FHL1 in the Differential Diagnosis of Papillary Thyroid Carcinoma and Benign Tumors.
- Published in:
- Journal of Isfahan Medical School, 2014, v. 31, n. 266, p. 1
- By:
- Publication type:
- Article