Associated Papers
Expanding the phenotypic spectrum associated with CFAP43 mutations: a case report of familial male infertility with respiratory manifestations.
Awad F et al.
Frontiers in Reproductive Health, 2025
41341611 (PubMed )
Supplement: Datasheet1.xlsx › Patient_1
Genetic Variants Linked to Dyslexia Co-Morbid ADHD: A Case Study of a Pakistani Outpatient.
Haider S et al.
Journal of Population Therapeutics and Clinical Pharmacology = Journal De La Therapeutique Des Populations Et De La Pharmacologie Clinique, 2024
Association of SNPs of DYX1C1 with developmental dyslexia in an Indian population.
Venkatesh SK et al.
Psychiatric Genetics, 2014
Approach to epigenetic analysis in language disorders.
Smith SD
Journal of Neurodevelopmental Disorders, 2011
Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population.
Paracchini S et al.
Genes, Brain, and Behavior, 2011
An examination of candidate gene SNPs for dyslexia in an Indian sample.
Venkatesh SK et al.
Behavior Genetics, 2011
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