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Journal Article
Nature, ISSN 0028-0836, 10/2011, Volume 478, Issue 7367, pp. 57 - 63
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2015, Volume 10, Issue 8, pp. e0129631 - e0129631
Journal Article
Molecular Psychiatry, ISSN 1359-4184, 01/2018, Volume 24, Issue 7, pp. 1 - 13
Journal Article
Journal of Optics (United Kingdom), ISSN 2040-8978, 05/2018, Volume 20, Issue 5, p. 54005
Journal Article
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, ISSN 1552-4841, 12/2018, Volume 177, Issue 8, pp. 691 - 699
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 01/2019, Volume 179, Issue 1, pp. 13 - 19
Intellectual disability (ID), a genetically and clinically heterogeneous disorder, affects 1%–3% of the general population and is a major health problem,... 
microcephaly | GPR126 | cerebellar hypoplasia | intellectual disability | WHITE-MATTER | PHENOTYPE | PROTEIN-COUPLED RECEPTORS | PHARMACOLOGY | GENETICS & HEREDITY | OXYTOCIN | SCHWANN-CELLS | GRAY-MATTER | BRAIN | Hypoplasia | Cerebellum | Myelination | Microencephaly | Intellectual disabilities | Schwann cells | Developing countries | Spasticity | Id protein | Seizures
Journal Article
Procedia - Social and Behavioral Sciences, ISSN 1877-0428, 05/2014, Volume 98, pp. 1698 - 1705
Academic texts are characterized by the use of longer minimal terminal units (t-units) containing complex grammatical structures and various clause types. The... 
Academic Writing | Clause | Minimum terminal unit (t-unit) | Grammatical Complexity
Journal Article
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, ISSN 1552-4841, 12/2018, Volume 177, Issue 8, pp. 691 - 699
Journal Article
Neuromuscular Disorders, ISSN 0960-8966, 2016, Volume 26, Issue 4, pp. 277 - 282
Highlights • Whole exome sequencing (WES) was performed for 6 unrelated Iranian probands diagnosed with a kind of muscular disorder. • Mutations in CAPN3 gene... 
Neurology | Calpain3 | CAPN3 | Limb-girdle | Iran | Whole exome sequencing | Muscular dystrophy | CALPAIN-3 | MUSCLE | NEUROSCIENCES | CLINICAL NEUROLOGY | FREQUENCY | MUTATIONS | LGMD2A | Sequence Deletion | Exons | Humans | Male | Calpain - genetics | Muscle Proteins - genetics | Young Adult | DNA Mutational Analysis | Muscular Dystrophies, Limb-Girdle - genetics | Pedigree | Base Sequence | Adolescent | Adult | Family | Female | Genetic research | Genes | Index Medicus
Journal Article
Journal of Human Genetics, ISSN 1434-5161, 2014, Volume 59, Issue 7, pp. 368 - 375
Bardet-Biedl syndrome (BBS) is a rare ciliopathy disorder that is clinically and genetically heterogeneous with 18 known genes. This study was performed to... 
DIAGNOSIS | COMPLEX | OBESITY | DISEASES | DATABASE | DNA | GENETICS & HEREDITY | IDENTIFICATION | FAMILY | Amino Acid Sequence | Humans | Molecular Sequence Data | Genotype | Male | Genetic Heterogeneity | Phenotype | Sequence Alignment | Iran | DNA Mutational Analysis | Base Sequence | Bardet-Biedl Syndrome - genetics | Female | Consanguinity | Mutation | Quantitative Trait Loci | Index Medicus
Journal Article