Human Genome Epidemiology Literature Finder
Records 1 - 6 (of 6 Records) |
Query Trace: Syndrome and FRAXE[original query] |
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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 |
[Polymorphism of trinucleotide repeats at loci FRAXA and FRAXE in the population of Tomsk]. Genetika 2002 Feb 38 (2): 268-73. Tolmacheva E N, Nazarenko S |
Genetic and neurological evaluation in a sample of individuals with pervasive developmental disorders. Arquivos de neuro-psiquiatria 2003 Jun 61 (2A): 176-80. Steiner Carlos Eduardo, Guerreiro Marilisa Mantovani, Marques-de-Faria Antonia Pau |
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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