(Q41684133)

7 October 2017

title

Periodic hypokalemic paralysis transmitted by an unaffected male with negative family history: a delayed mutation? (English)

1 reference

7 October 2017

Periodic hypokalemic paralysis transmitted by an unaffected male with negative family history: A delayed mutation? (English)

1 reference

21 May 2023

1 reference

21 May 2023

author name string

H. H. Ropers

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A457125

3 July 2022

H. B. Szliwowski

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A457125

3 July 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=457125

3 July 2022

publication date

1 April 1979

1 reference

7 October 2017

17 April 1979

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=457125

full work available at URL

3 July 2022

http://link.springer.com/content/pdf/10.1007/BF00273282.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF00273282/fulltext.html

21 May 2023

1 reference

http://link.springer.com/content/pdf/10.1007/BF00273282

21 May 2023

1 reference

21 May 2023

1 reference

7 October 2017

volume

48

1 reference

7 October 2017

issue

1

1 reference

7 October 2017

page(s)

113-116

1 reference

https://scigraph.springernature.com/pub.10.1007/bf00273282

7 October 2017

exact match

0 references

cites work

Letter: Half chromatid mutations may explain incontinentia pigmenti in males

1 reference

12 December 2020

Mutation in eukaryotes

1 reference

12 December 2020

Clinical features of hereditary transient paralysis; periodic adynamia and periodic paralysis

1 reference

12 December 2020

X-linked mental retardation: Transmission of the trait by an apparently unaffected male

1 reference

12 December 2020

Hereditary transient muscular paralysis in Denmark; genetic aspects of family periodic paralysis and family periodic adynamia.

1 reference

12 December 2020

Letter: Heterogenic monozygocity: evidence for the transmission of half chromatid mutations in humans?

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00273282

1 reference

Dimensions Publication ID

7 October 2017

1013383433

0 references

1 reference