Human Genome Epidemiology Literature Finder
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Records 1 - 13 (of 13 Records) |
| Query Trace: Fragile X Syndrome 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 |
| 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 |
| 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 |
| Is the 31 CAG repeat allele of the spinocerebellar ataxia 1 (SCA1) gene locus non-specifically associated with trinucleotide expansion diseases? Psychiatric genetics 2001 Dec 11 (4): 201-5. Savi? D, Topisirovi? I, Keckarevi? M, Keckarevi? D, Major T, Culjkovi? B, Stojkovi? O, Rakocevi?-Stojanovi? V, Mladenovi? J, Todorovi? S, Apostolski S, Romac |
| 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 |
| 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 |
| Cytogenetic abnormalities and fragile-X syndrome in Autism Spectrum Disorder. BMC medical genetics 2005 1 6 3. Reddy Kavita |
| An investigation of FRAXA intermediate allele phenotype in a longitudinal sample. Annals of human genetics 2006 Mar 70 (Pt 2): 170-80. Ennis S, Murray A, Youings S, Brightwell G, Herrick D, Ring S, Pembrey M, Morton N E, Jacobs P |
| Analysis of the Fragile X Trinucleotide Repeat in Basques: Association of Premutation and Intermediate Sizes, Anchoring AGGs and Linked Microsatellites with Unstable Alleles. Current genomics 2008 May 9 (3): 191-9. Arrieta M I, Ramírez J M, Télez M, Flores P, Criado B, Barasoain M, Huerta I, González A |
| 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? |
| 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 |
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