X-linked Duchenne muscular dystrophy in an unusual family with manifesting carriers (Q70646328)

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scientific article published on 01 January 1984

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Language	Label	Description	Also known as
English	X-linked Duchenne muscular dystrophy in an unusual family with manifesting carriers	scientific article published on 01 January 1984

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6490012

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6490012%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

title

X-linked Duchenne muscular dystrophy in an unusual family with manifesting carriers (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6490012

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6490012%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

main subject

Duchenne muscular dystrophy

1 reference

based on heuristic

inferred from title

author name string

B Kaladhar Reddy

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6490012

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6490012%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

T E Anandavalli

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6490012

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6490012%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

O S Reddi

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6490012

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6490012%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

publication date

1 January 1984

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6490012

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6490012%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

published in

Human Genetics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6490012

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6490012%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

volume

67

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6490012

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6490012%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

issue

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6490012

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6490012%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

page(s)

460-462

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6490012

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6490012%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

cites work

Muscular dystrophy in young girls.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6490012

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Formal genetics of muscular dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6490012

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6490012

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SEVERE MUSCULAR DYSTROPHY IN GIRLS

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6490012

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary myopathies

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6490012

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscular dystrophy in Northern Ireland, I. An account of the condition in fifty-one families

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6490012

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Failure of inactivation of Duchenne dystrophy X-chromosome in one of female identical twins

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6490012

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6490012

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duchenne muscular dystrophy. A population study

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6490012

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duchenne muscular dystrophy in young girls?

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6490012

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sex chromatin and gene action in the mammalian X-chromosome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6490012

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscular dystrophy in young girls

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6490012

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The inheritance of muscular dystrophy: further observations

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6490012

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gene action in the X-chromosome of the mouse (Mus musculus L.)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6490012

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6490012

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-chromosome mosaicism in females with muscular dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6490012

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MUSCULAR DYSTROPHY (DUCHENNE) IN A GIRL WITH TURNER'S SYNDROME.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/6490012

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF00291412

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6490012

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6490012%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

PubMed publication ID

6490012

1 reference

stated in

Europe PubMed Central

PubMed publication ID

6490012

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6490012%20AND%20SRC:MED&resulttype=core&format=json

retrieved

12 October 2019

 

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