Genetic counselling in facioscapulohumeral muscular dystrophy (Q33597601)

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Language	Label	Description	Also known as
English	Genetic counselling in facioscapulohumeral muscular dystrophy	scientific article

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1941962

retrieved

28 July 2017

title

Genetic counselling in facioscapulohumeral muscular dystrophy (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1941962

retrieved

28 July 2017

main subject

facioscapulohumeral muscular dystrophy

0 references

author name string

Lunt PW

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1941962

retrieved

28 July 2017

Harper PS

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1941962

retrieved

28 July 2017

language of work or name

English

0 references

publication date

1 October 1991

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1941962

retrieved

28 July 2017

published in

Journal of Medical Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1941962

retrieved

28 July 2017

volume

28

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1941962

retrieved

28 July 2017

issue

10

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1941962

retrieved

28 July 2017

page(s)

655-664

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1941962

retrieved

28 July 2017

cites work

Formal genetics of muscular dystrophy

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017051

retrieved

14 July 2018

Genetic-epidemiological studies in progressive muscular dystrophy

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017051

retrieved

14 July 2018

The facio-scapulo-limb (or the facioscapulohumeral) type of muscular dystrophy. Clinical and genetic study of 200 cases.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017051

retrieved

14 July 2018

Facioscapulohumeral dystrophy presenting in infancy with facial diplegia and sensorineural deafness

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017051

retrieved

14 July 2018

Hearing loss in facioscapulohumeral dystrophy

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017051

retrieved

14 July 2018

Retinal vascular abnormalities in facioscapulohumeral muscular dystrophy. A general association with genetic and therapeutic implications

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017051

retrieved

14 July 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017051

retrieved

14 July 2018

Linkage analysis in the spinal muscular atrophy type of facioscapulohumeral disease.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017051

retrieved

14 July 2018

Emotional facial paresis with striatocapsular infarction

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017051

retrieved

14 July 2018

Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017051

retrieved

14 July 2018

A closely linked DNA marker for facioscapulohumeral disease on chromosome 4q.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017051

retrieved

14 July 2018

Chronic spinal muscular atrophy of facioscapulohumeral type

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017051

retrieved

14 July 2018

Coats' disease and muscular dystrophy

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017051

retrieved

30 October 2018

Neurogenic atrophy simulating facioscapulohumeral dystrophy. A dominant form

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1941962

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Creatine Phosphokinase in Facioscapulohumeral Muscular Dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1941962

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The myogenic scapulo-peroneal syndrome. Muscular dystrophy in the K. kindred: clinical study and genetics

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1941962

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Thoracoscapular fusion for facioscapulohumeral dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1941962

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Death in childhood due to facio-scapulo-humeral dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1941962

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Infantile facioscapulohumeral muscular dystrophy: new observations

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1941962

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA probes in differential diagnosis of Becker muscular dystrophy and spinal muscular atrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1941962

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Xp21 DNA PROBE IN DIAGNOSIS OF MUSCULAR DYSTROPHY AND SPINAL MUSCULAR ATROPHY

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1941962

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA marker applicable to presymptomatic and prenatal diagnosis of facioscapulohumeral disease

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1941962

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1136/JMG.28.10.655

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1941962

retrieved

28 July 2017

PMC publication ID

1017051

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1941962

retrieved

28 July 2017

PubMed publication ID

1941962

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1941962

retrieved

28 July 2017

ResearchGate publication ID

21213956

0 references

 

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