Application of chromosome 4q35-qter marker (pFR-1) for DNA rearrangement of facioscapulohumeral muscular dystrophy patients in Taiwan (Q73378668)

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3 November 2019

title

Application of chromosome 4q35-qter marker (pFR-1) for DNA rearrangement of facioscapulohumeral muscular dystrophy patients in Taiwan (English)

1 reference

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facioscapulohumeral muscular dystrophy

3 November 2019

main subject

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author name string

Y D Hsu

1

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3 November 2019

M C Kao

2

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3 November 2019

W C Shyu

3

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3 November 2019

J C Lin

4

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3 November 2019

N E Huang

5

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3 November 2019

H F Sun

6

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3 November 2019

K D Yang

7

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3 November 2019

W L Tsao

8

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publication date

1 July 1997

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Journal of the Neurological Sciences

3 November 2019

published in

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volume

149

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3 November 2019

issue

1

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3 November 2019

page(s)

73-79

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DNA rearrangements in Japanese facioscapulohumeral muscular dystrophy patients: clinical correlations

3 November 2019

cites work

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Genetics of facioscapulohumeral muscular dystrophy: new mutations in sporadic cases

7 January 2021

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A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies

7 January 2021

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Estimation of age dependent penetrance in facioscapulohumeral muscular dystrophy by minimising ascertainment bias

7 January 2021

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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)

7 January 2021

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Inflammatory myopathy with facioscapulohumeral distribution

7 January 2021

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Facioscapulohumeral muscular dystrophy in the Dutch population

7 January 2021

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No evidence of genetic heterogeneity in Brazilian facioscapulohumeral muscular dystrophy familes (FSHD) with 4q markers

7 January 2021

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Extreme variability of expression in monozygotic twins with FSH muscular dystrophy

7 January 2021

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Scapuloperoneal syndromes. Absence of linkage to the 4q35 FSHD locus

7 January 2021

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Evidence for anticipation and association of deletion size with severity in facioscapulohumeral muscular dystrophy. The FSH-DY Group

7 January 2021

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Molecular analysis of British facioscapulohumeral dystrophy families for 4q DNA rearrangements

7 January 2021

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FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandemly repeated unit

7 January 2021

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Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35

7 January 2021

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Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromosome 4q35 recombination events

7 January 2021

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Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.

7 January 2021

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Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization

7 January 2021

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Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

7 January 2021

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Molecular genetics of facioscapulohumeral muscular dystrophy

7 January 2021

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10.1016/S0022-510X(97)05394-X

7 January 2021

Identifiers

DOI

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3 November 2019

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