Human Genome Epidemiology Literature Finder
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Records 1 - 14 (of 14 Records) |
| Query Trace: Mental Retardation and FRAXA[original query] |
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| [Molecular diagnosis of fragile X syndrome with polymerase chain reaction: application of a diagnostic protocol in 50 families from northern Spain]. Anales españoles de pediatría 2001 Apr 54 (4): 331-9. Durán Domínguez M, Molina Carrillo M, Fernández Toral J, Martínez Merino T, López Arístegui MA, Alvarez Retuerto AI, Onaindía Urquijo ML, Tejada Mínguez MI |
| FRAXA screening in Brazilian institutionalized individuals with nonspecific severe mental retardation. Genetic testing 2000 4 (3): 283-7. Mulatinho M V, Llerena J C, Pimentel M |
| [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 |
| Fragile X premutation in women with sporadic premature ovarian failure in Slovenia. Human reproduction (Oxford, England) 2003 Aug 18 (8): 1637-40. Gersak Ksenija, Meden-Vrtovec Helena, Peterlin Bor |
| Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardation. Journal of neurogenetics 0 17 (2-3): 223-30. Major Tamara, Culjkovic Biljana, Stojkovic Oliver, Gucscekic Marija, Lakic Aneta, Romac Stan |
| MECP2 mutations or polymorphisms in mentally retarded boys: diagnostic implications. Molecular diagnosis : a journal devoted to the understanding of human disease through the clinical application of molecular biology 2003 7 (1): 3-7. Bourdon Violaine, Philippe Christophe, Martin Dominique, Verloès Alain, Grandemenge Agnès, Jonveaux Philip |
| Genetic diversity at the FMR1 locus in Mexican population. Archives of medical research 0 36 (4): 412-7. Rosales-Reynoso Mónica Alejandra, Mendoza-Carrera Francisco, Troyo-Sanromán Rogelio, Medina Claudina, Barros-Núñez Patric |
| Mutation screening of the MECP2 gene in a large cohort of 613 fragile-X negative patients with mental retardation. European journal of medical genetics 0 50 (3): 200-8. Lesca Gaëtan, Bernard Virginie, Bozon Muriel, Touraine Renaud, Gérard Daniel, Edery Patrick, Calender Ala |
| Haplotype analysis at the FRAXA locus in an Indian population. American journal of medical genetics. Part A 2008 Aug 146A (15): 1980-5. Chakraborty S Saha, Mondal Bama Charan, Das S, Das K, Dasgupta U |
| Haplotype and AGG interspersion analysis of FMR1 alleles in a Croatian population: no founder effect detected in patients with fragile X syndrome. Human biology 2008 Oct 80 (5): 581-7. Doki? H, Barisi? I, Culi? V, Lozi? B, He?imovi? |
| Intermediate alleles at the FRAXA and FRAXE loci in Parkinson's disease. Parkinsonism & related disorders 2011 May 17 (4): 281-4. Costa Alzenira, Gao Lin, Carrillo Fátima, Cáceres-Redondo María Teresa, Carballo Manuel, Díaz-Martín Juan, Gómez-Garre Pilar, Sobrino Francisco, Lucas Miguel, López-Barneo José, Mir Pablo, Pintado Elizabe |
| 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 |
| Distribution of fragile X mental retardation 1 CGG repeat and flanking haplotypes in a large Chinese population. Molecular genetics & genomic medicine 2015 May 3 (3): 172-81. Huang Wen, Xia Qiuping, Luo Shiyu, He Hua, Zhu Ting, Du Qian, Duan Ranh |
| Haplotype Analysis of DXS548 and FRAXAC1 Microsatellite Loci in Iranian Patients with Fragile X Syndrome. Iranian journal of child neurology 2018 12 (1): 36-46. Aleyasin Seyed Ahmad, Salamat Fatemeh, Mirakhori Mojg |
- Page last reviewed:Feb 1, 2024
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