(Q69890439)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878115%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

title

DNA analysis for ornithine transcarbamylase deficiency (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878115%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

author name string

R Rozen

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878115%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

J E Fox

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878115%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

A M Hack

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878115%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

W A Fenton

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878115%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

A L Horwich

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878115%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

L E Rosenberg

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878115%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

publication date

1 January 1986

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878115%20AND%20SRC:MED&resulttype=core&format=json

Journal of Inherited Metabolic Disease

6 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878115%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

volume

9 Suppl 1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878115%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

page(s)

49-57

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2878115%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf01800858

6 October 2019

exact match

0 references

cites work

Fetal liver biopsy for prenatal diagnosis of ornithine carbamyl transferase deficiency

1 reference

12 December 2020

Evidence for x-linked dominant inheritance of ornithine transcarbamylase deficiency.

1 reference

12 December 2020

Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis

1 reference

12 December 2020

Gene deletion and restriction fragment length polymorphisms at the human ornithine transcarbamylase locus

1 reference

12 December 2020

Human ornithine transcarbamylase locus mapped to band Xp21.1 near the Duchenne muscular dystrophy locus

1 reference

12 December 2020

X-chromosome inactivation in human liver: confirmation of X-linkage of ornithine transcarbamylase

1 reference

12 December 2020

Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome

1 reference

12 December 2020

Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome

1 reference

12 December 2020

Prenatal diagnosis of ornithine transcarbamylase deficiency utilizing fetal liver biopsy.

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

Structure and Expression of a Complementary DNA for the Nuclear Coded Precursor of Human Mitochondrial Ornithine Transcarbamylase

1 reference

12 December 2020