Pages that link to "Q70732388"

The following pages link to The identification of a third fragile site, FRAXF, in Xq27--q28 distal to both FRAXA and FRAXE (Q70732388):

Displaying 24 items.

• FRAXE and mental retardation (Q24517881) (← links)
• FRAXF in a patient with chromosome 8 duplication (Q33677585) (← links)
• Fragile X syndrome is less common than previously estimated (Q33678232) (← links)
• Clinical, cytogenetic, and molecular analysis of three families with FRAXE (Q33678260) (← links)
• CGG repeats associated with DNA instability and chromosome fragility form structures that block DNA synthesis in vitro (Q34777507) (← links)
• X-linked mental retardation: vanishing boundaries between non-specific (MRX) and syndromic (MRXS) forms (Q35026980) (← links)
• Analysis of a CGG sequence at the FMR-1 locus in fragile X families and in the general population (Q35195212) (← links)
• A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom. (Q35881640) (← links)
• Expansion and methylation status at FRAXE can be detected on EcoRI blots used for FRAXA diagnosis: analysis of four FRAXE families with mild mental retardation in males (Q35882071) (← links)
• Triplet repeat expansion at the FRAXE locus and X-linked mild mental handicap. (Q35889234) (← links)
• Segregation of FRAXE in a large family: clinical, psychometric, cytogenetic, and molecular data (Q35889580) (← links)
• A panel of deleted mouse X chromosome somatic cell hybrids derived from the embryonic stem cell line HD3 shows preferential breakage in the Hprt-DXHX254E region. (Q38313640) (← links)
• DNA analysis in forensics, disease and animal/plant identification (Q40534331) (← links)
• A novel gene, FAM11A, associated with the FRAXF CpG island is transcriptionally silent in FRAXF full mutation (Q40693826) (← links)
• Huntington disease: Advances in molecular and cell biology (Q41521368) (← links)
• Screening for Fragile X Syndrome: Information Needs for Health Planners (Q41579814) (← links)
• The DMPK Gene of Severely Affected Myotonic Dystrophy Patients Is Hypermethylated Proximal to the Largely Expanded CTG Repeat (Q41968306) (← links)
• Autism spectrum disorder: FRAXE mutation, a rare etiology (Q50305806) (← links)
• Autism and the X chromosome: no linkage to microsatellite loci detected using the affected sibling pair method (Q50309937) (← links)
• A simple multiplex FRAXA, FRAXE, and FRAXF PCR assay convenient for wide screening programs (Q51986224) (← links)
• Fragile X syndrome (Q72157963) (← links)
• Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE (Q72586906) (← links)
• Molecular diagnosis of the fragile X and FRAXE syndromes in patients with mental retardation of unknown cause in Mexico (Q73807864) (← links)
• The fragile X syndrome (Q74809876) (← links)