Frequency of FMR1 gene mutation and CGG repeat polymorphism in intellectually disabled children in Pakistan - Fatima, Tasneem; Zaidi, Syed Aley Hasan; Sarfraz, Noorjehan; Perween, Siddiqa; Khurshid, Faraz; Imtiaz, Fauzia (American journal of medical genetics. Part A, 2014)
Keywords: Adolescent; Alleles; Biradri (community of same cast or kinship); Biradri (community of same cast or kinship), consanguinity; Case-Control Studies; CGG repeats; Child; Child, Preschool; consanguinity; Female; FMR1 gene; FMRP; Fragile X Mental Retardation Protein - genetics; fragile X syndrome; Fragile X Syndrome - diagnosis; Fragile X Syndrome - epidemiology; Fragile X Syndrome - genetics; Gene Frequency; Humans; intellectual disability; Male; methylation; Mutation; Pakistan; Polymorphism, Genetic; prevalence; Sequence Analysis, DNA; Trinucleotide Repeat Expansion; Pakistan; prevalence; Pakistan; Biradri (community of same cast or kinship), consanguinity; FMRP; methylation; fragile X syndrome; CGG repeats; intellectual disability; FMR1 gene