Pages that link to "Q47382658"

The following pages link to Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletions (Q47382658):

Displaying 37 items.

• The Facioscapulohumeral muscular dystrophy region on 4qter and the homologous locus on 10qter evolved independently under different evolutionary pressure (Q24680328) (← links)
• Molecular genetics of facioscapulohumeral muscular dystrophy (FSHD) (Q28236842) (← links)
• De novo facioscapulohumeral muscular dystrophy defined by DNA probe p13E-11 (D4F104S1). (Q33625003) (← links)
• Direct detection of 4q35 rearrangements implicated in facioscapulohumeral muscular dystrophy (FSHD) (Q33677292) (← links)
• Improved molecular diagnosis of facioscapulohumeral muscular dystrophy (FSHD): validation of the differential double digestion for FSHD (Q33678953) (← links)
• Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial cases (Q33683060) (← links)
• Facioscapulohumeral muscular dystrophy (Q33790247) (← links)
• Myoblasts from affected and non-affected FSHD muscles exhibit morphological differentiation defects (Q34022975) (← links)
• Methylation of the FSHD syndrome-linked subtelomeric repeat in normal and FSHD cell cultures and tissues (Q34101814) (← links)
• Sequence homology between 4qter and 10qter loci facilitates the instability of subtelomeric KpnI repeat units implicated in facioscapulohumeral muscular dystrophy (Q34386097) (← links)
• Molecular diagnosis of facioscapulohumeral muscular dystrophy (Q34606340) (← links)
• Facioscapulohumeral Muscular Dystrophy: More Complex than it Appears (Q34685919) (← links)
• High proportion of new mutations and possible anticipation in Brazilian facioscapulohumeral muscular dystrophy families (Q35643770) (← links)
• Epigenetics and human disease (Q35918584) (← links)
• Alternative splicing and muscular dystrophy. (Q36599506) (← links)
• Physical Mapping Evidence for a Duplicated Region on Chromosome 10qter Showing High Homology with the Facioscapulohumeral Muscular Dystrophy Locus on Chromosome 4qter (Q36684384) (← links)
• Focal and other unusual presentations of facioscapulohumeral muscular dystrophy (Q38036090) (← links)
• RNAPol-ChIP analysis of transcription from FSHD-linked tandem repeats and satellite DNA. (Q42174305) (← links)
• [Clinical and molecular diagnosis of facioscapulohumeral dystrophy type 1 (FSHD1) in 2012]. (Q45979333) (← links)
• Correlation between fragment size at D4F104S1 and age at onset or at wheelchair use, with a possible generational effect, accounts for much phenotypic variation in 4q35-facioscapulohumeral muscular dystrophy (FSHD) (Q47354966) (← links)
• The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes (Q48071488) (← links)
• Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy (Q48080420) (← links)
• Equal proportions of affected cells in muscle and blood of a mosaic carrier of facioscapulohumeral muscular dystrophy. (Q51828623) (← links)
• Facioscapulohumeral Muscular Dystrophy. (Q52506936) (← links)
• Analysis of the organisation and localisation of the FSHD-associated tandem array in primates: implications for the origin and evolution of the 3.3 kb repeat family (Q71468182) (← links)
• Phenotypic-genotypic correlation will assist genetic counseling in 4q35-facioscapulohumeral muscular dystrophy (Q72213895) (← links)
• Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35 (Q72213898) (← links)
• Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35 (Q72213904) (← links)
• Efforts toward understanding the molecular basis of facioscapulohumeral muscular dystrophy (Q72213909) (← links)
• The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qter (Q72213912) (← links)
• Germinal mosaicism in facioscapulohumeral muscular dystrophy (FSHD) (Q72213917) (← links)
• Characterization of a tandemly repeated 3.3-kb KpnI unit in the facioscapulohumeral muscular dystrophy (FSHD) gene region on chromosome 4q35 (Q72213930) (← links)
• Facioscapulohumeral muscular dystrophy in the Dutch population (Q72213941) (← links)
• Prenatal diagnosis for facioscapulohumeral muscular dystrophy (FSHD) (Q73084000) (← links)
• Molecular analysis of 4q35 rearrangements in fascioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the disease (Q77925406) (← links)
• Increased levels of adenine nucleotide translocator 1 protein and response to oxidative stress are early events in facioscapulohumeral muscular dystrophy muscle (Q81024511) (← links)
• Analyzing Copy Number Variation Using Pulsed-Field Gel Electrophoresis: Providing a Genetic Diagnosis for FSHD1 (Q88714539) (← links)