(Q24514921)

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An unusual family of benign "X" linked muscular dystrophy with cardiac involvement

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title

An unusual family of benign "X" linked muscular dystrophy with cardiac involvement (English)

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R S Wadia

1

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S U Wadgaonkar

series ordinal

2

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R B Amin

series ordinal

3

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H V Sardesai

series ordinal

4

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language of work or name

English

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publication date

October 1976

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published in

Journal of Medical Genetics

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volume

13

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issue

5

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page(s)

352-6

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cites work

Unusual type of benign x-linked muscular dystrophy

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1013439

retrieved

19 March 2017

Slowly progressive X-linked recessive muscular dystrophy (type 3b). Report of cases and review of the literature

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=1013439

retrieved

27 September 2017

Abnormalities of the electrocardiogram in hereditary myopathies

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=1013439

retrieved

27 September 2017

Linkage between the loci for benign (Becker-type) X-borne muscular dystrophy and deutan colour blindness

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=1013439

retrieved

27 September 2017

X-linked scapuloperoneal syndrome

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=1013439

retrieved

27 September 2017

Myocardial Involvement in Benign Duchenne Type of Progressive Muscular Dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1003445

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New type of recessive X-linked muscular dystrophy: scapulo-humeral-distal muscular dystrophy with early contractures and cardiac arrhythmias

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1003445

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked pseudohypertrophic muscular dystrophy with a late onset and slow progression

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1003445

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The electrocardiogram in Duchenne progressive muscular dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1003445

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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PubMed publication ID

1003445

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ResearchGate publication ID

22152421

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(Q24514921)

An unusual family of benign "X" linked muscular dystrophy with cardiac involvement

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