Becker muscular dystrophy (BMD) and Klinefelter's syndrome: a possible cause of variable expression of BMD within a pedigree (Q33598438)

28 July 2017

title

Becker muscular dystrophy (BMD) and Klinefelter's syndrome: a possible cause of variable expression of BMD within a pedigree (English)

1 reference

28 July 2017

main subject

Klinefelter's syndrome

1 reference

Becker muscular dystrophy

inferred from title

1 reference

Suthers GK

1

1 reference

28 July 2017

Manson JI

2

1 reference

28 July 2017

Stern LM

3

1 reference

28 July 2017

Haan EA

4

1 reference

28 July 2017

Mulley JC

5

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 April 1989

1 reference

Journal of Medical Genetics

28 July 2017

published in

1 reference

28 July 2017

volume

26

1 reference

28 July 2017

issue

4

1 reference

28 July 2017

page(s)

251-254

1 reference

Sex chromatin pattern in seminiferous tubule dysgenesis and other testicular disorders: relationship to true hermaphrodism and to Klinefelter's syndrome, with a review of gonadal ontogenesis

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017298

Muscular dystrophy in girls with X;autosome translocations

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017298

Population data on benign and severe forms of X-linked muscular dystrophy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017298

An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017298

Duchenne muscular dystrophy in one of monozygotic twin girls

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017298

The detection of carriers of benign (Becker-type) X-linked muscular dystrophy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017298

Clinical studies in benign (Becker type) X-linked muscular dystrophy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017298

X-Linked muscular dystrophy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017298

Intrafamilial variability of X-linked progressive muscular dystrophy. Mild and acute form of X-linked muscular dystrophy in the same family

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017298

Detection of carriers of benign X-linked muscular dystrophy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1017298

Inherited deletion at Duchenne dystrophy locus in normal male

30 October 2018

1 reference

12 December 2020

Preferential deletion of exons in Duchenne and Becker muscular dystrophies

1 reference

12 December 2020

Biochemical, histological and clinical findings in a four-year-old female carrier of benign X-linked muscular dystrophy (Becker type)

1 reference

12 December 2020

Intellectual functioning in non-Duchenne muscular dystrophy

1 reference

12 December 2020

The inheritance of muscular dystrophy: further observations

1 reference

12 December 2020

Identifiers

PMC publication ID

1017298

1 reference

28 July 2017

1 reference