(Q64050276)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9171836%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

title

Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9171836%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference

Mansfield TA

1

1 reference

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3 November 2019

Simon DB

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9171836%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Farfel Z

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9171836%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Bia M

4

1 reference

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3 November 2019

Tucci JR

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9171836%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Lebel M

6

1 reference

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3 November 2019

Gutkin M

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9171836%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Vialettes B

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9171836%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

Christofilis MA

9

1 reference

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3 November 2019

Kauppinen-Makelin R

10

1 reference

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3 November 2019

Mayan H

11

1 reference

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3 November 2019

Risch N

12

1 reference

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3 November 2019

Lifton RP

13

1 reference

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3 November 2019

language of work or name

English

0 references

publication date

1 June 1997

1 reference

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3 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9171836%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

volume

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9171836%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

issue

2

1 reference

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3 November 2019

page(s)

202-205

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9171836%20AND%20SRC:MED&resulttype=core&format=json

Molecular genetics of human blood pressure variation

3 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-202

7 January 2021

HYPERTENSION AND HYPERPOTASSAEMIA WITHOUT RENAL DISEASE IN A YOUNG MALE

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-202

7 January 2021

Mineralocorticoid-resistant renal hyperkalemia without salt wasting (type II pseudohypoaldosteronism): role of increased renal chloride reabsorption.

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-202

7 January 2021

Familial hyperpotassemia and hypertension accompanied by normal plasma aldosterone levels: possible hereditary cell membrane defect

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-202

7 January 2021

Type II pseudohypoaldosteronism. Report of a case and review of the literature

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-202

7 January 2021

Endocrine sodium and volume regulation in familial hyperkalemia with hypertension

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-202

7 January 2021

A deficient response of atrial natriuretic peptide to volume overload in Gordon's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-202

7 January 2021

Genetic mapping of a gene causing hypertension in the stroke-prone spontaneously hypertensive rat

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-202

7 January 2021

Chromosomal mapping of two genetic loci associated with blood-pressure regulation in hereditary hypertensive rats

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-202

7 January 2021

Localisation of pseudohypoaldosteronism genes to chromosome 16p12.2-13.11 and 12p13.1-pter by homozygosity mapping

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-202

7 January 2021

Polymorphic DNA region adjacent to the 5' end of the human insulin gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-202

7 January 2021

Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-202

7 January 2021

Avoiding recomputation in linkage analysis.

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-202

7 January 2021

Strategies for multilocus linkage analysis in humans

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-202

7 January 2021

Integrating Parallelization Strategies for Linkage Analysis

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-202

7 January 2021

TreadMarks: shared memory computing on networks of workstations

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-202

7 January 2021

The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance

1 reference

https://api.crossref.org/works/10.1038%2FNG0697-202

7 January 2021

Identifiers

DOI

10.1038/NG0697-202

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9171836%20AND%20SRC:MED&resulttype=core&format=json

3 November 2019

1 reference