Found: 9
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Whole Genome Analysis in Consanguineous Families Reveals New Loci for Speech Sound Disorder (SSD).
- Published in:
- Genes, 2024, v. 15, n. 8, p. 1069, doi. 10.3390/genes15081069
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- Article
Identification of an autosomal recessive stuttering locus on chromosome 3q13.2–3q13.33.
- Published in:
- 2010
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- Publication type:
- Report
Family-Based Whole-Exome Analysis of Specific Language Impairment (SLI) Identifies Rare Variants in BUD13 , a Component of the Retention and Splicing (RES) Complex.
- Published in:
- Brain Sciences (2076-3425), 2022, v. 12, n. 1, p. 47, doi. 10.3390/brainsci12010047
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- Article
A missense variant of the ATP1A2 gene is associated with a novel phenotype of progressive sensorineural hearing loss associated with migraine.
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- European Journal of Human Genetics, 2015, v. 23, n. 5, p. 639, doi. 10.1038/ejhg.2014.154
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- Article
Pedigree-Based Gene Mapping Supports Previous Loci and Reveals Novel Suggestive Loci in Specific Language Impairment.
- Published in:
- Journal of Speech, Language & Hearing Research, 2020, v. 63, n. 12, p. 4046, doi. 10.1044/2020_JSLHR-20-00102
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- Publication type:
- Article
NEEDLE STICK INJURIES IN HEALTHCARE WORKERS OF A SECONDARY CARE HOSPITAL, PAKISTAN.
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- Professional Medical Journal, 2020, v. 27, n. 3, p. 552, doi. 10.29309/tpmj/2020.27.03.3565
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- Publication type:
- Article
DIAGNOSTIC ACCURACY OF BEDSIDE INDEX OF SEVERITY IN ACUTE PANCREATITIS SCORE IN PREDICTING OUTCOMES IN PATIENTS PRESENTING WITH ACUTE PANCREATITIS.
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- Pakistan Armed Forces Medical Journal, 2020, v. 70, n. 5, p. 1511
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- Publication type:
- Article
Innovative Family-Based Genetically Informed Series of Analyses of Whole-Exome Data Supports Likely Inheritance for Grammar in Children with Specific Language Impairment.
- Published in:
- Children, 2023, v. 10, n. 7, p. 1119, doi. 10.3390/children10071119
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- Publication type:
- Article
A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures.
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- Human Molecular Genetics, 2021, v. 30, n. 12, p. 1160, doi. 10.1093/hmg/ddab111
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- Publication type:
- Article