Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy (Q69896114)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2881877%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

title

Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2881877%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

1 reference

A P Monaco

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2881877%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

C J Bertelson

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2881877%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

C Colletti-Feener

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2881877%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

L M Kunkel

series ordinal

4

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6 October 2019

publication date

1 March 1987

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6 October 2019

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2881877%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

volume

75

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6 October 2019

issue

3

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2881877%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

page(s)

221-227

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2881877%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00281063

6 October 2019

exact match

0 references

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Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus.

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Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families

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

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Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs

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Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy

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Cytogenetic heterogeneity of translocations associated with Duchenne muscular dystrophy

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