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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 15, 2025. (Total: 235337Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Fragile X Syndrome and FRAXE[original query]
Expansion mutation frequency and CGG/GCC repeat polymorphism in FMR1 and FMR2 genes in an Indian population.
Genetic epidemiology 2001 Jan 20 (1): 129-144.
Sharma D, Gupta M, Thelma B
Haplotype analysis at the FRAXA locus in Thai subjects.
American journal of medical genetics 2001 Jan 98 (3): 224-9.
Limprasert P, Saechan V, Ruangdaraganon N, Sura T, Vasiknanote P, Jaruratanasirikul S, Brown W
Fragile X syndrome: a clinico-genetic study of mentally retarded patients in Kuwait.
Eastern Mediterranean health journal = La revue de santé de la Méditerranée orientale = al-Majallah al-?i???yah li-sharq al-mutawassi? 0 10 (1-2): 116-24.
Bastaki L A, Hegazy F, Al-Heneidi M M, Turki N, Azab A S, Naguib K
Distribution of CGG/GCC repeats at the FMR1 and FMR2 genes in an Indian population with mental retardation of unknown etiology.
Genetic testing and molecular biomarkers 2011 Apr 15 (4): 281-4.
Katikala Lavanya, Guruju Mallikarjuna R, Madireddi Sujatha, Vallamkonda Omsairamesh, Vallamkonda Nagaratna, Persha Amarjyothi, Spurgeon Anandaraj M P
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