(Q69891524)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878868%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

title

Localisation of the gene for Hunter syndrome on the long arm of X chromosome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878868%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

author name string

M Upadhyaya

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878868%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

M Sarfarazi

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878868%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

J S Bamforth

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878868%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

N S Thomas

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878868%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

I Oberle

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878868%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

I Young

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878868%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

P S Harper

7

1 reference

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6 October 2019

publication date

1 December 1986

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6 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878868%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

volume

74

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878868%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

page(s)

391-398

1 reference

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6 October 2019

issue

4

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf00280492

6 October 2019

exact match

0 references

cites work

Carrier detection in Hunter syndrome

1 reference

12 December 2020

Strategies for multilocus linkage analysis in humans

1 reference

12 December 2020

Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies

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12 December 2020

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants

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12 December 2020

Cloning of a representative genomic library of the human X chromosome after sorting by flow cytometry

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"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum

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A clinically useful DNA probe closely linked to haemophilia A

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12 December 2020

Genetic mapping and diagnosis of haemophilia A achieved through a BclI polymorphism in the factor VIII gene

1 reference

12 December 2020

Carrier detection in haemophilia B using two further intragenic restriction fragment length polymorphisms

1 reference

12 December 2020

The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency

1 reference

12 December 2020

Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes

1 reference

12 December 2020

Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21.

1 reference

12 December 2020

Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site.

1 reference

12 December 2020

The linkage relation of the loci for the Xm serum system and the X-linked form of Hurler's syndrome (Hunter's syndrome).

1 reference

12 December 2020

Hunter's disease in a girl: association with X:5 chromosomal translocation disrupting the Hunter gene

1 reference

12 December 2020

Characterisation and use of an intragenic polymorphic marker for detection of carriers of haemophilia B (factor IX deficiency).

1 reference

12 December 2020

First trimester prenatal diagnosis of adrenoleukodystrophy by determination of very long chain fatty acid levels and by linkage analysis to a DNA probe

1 reference

12 December 2020

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

1 reference

12 December 2020

Polyclonal antibodies against iduronate 2-sulphate sulphatase from human urine

1 reference

12 December 2020

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

1 reference

12 December 2020

The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase

1 reference

12 December 2020