X-linked hydrocephalus: clinical heterogeneity at a single gene locus. (Q48463221)

From Wikidata

Jump to navigation Jump to search

scientific article published in July 1992

edit

Language	Label	Description	Also known as
English	X-linked hydrocephalus: clinical heterogeneity at a single gene locus.	scientific article published in July 1992

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1396913

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1396913%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 September 2019

title

X-linked hydrocephalus: clinical heterogeneity at a single gene locus (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1396913

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1396913%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 September 2019

main subject

hydrocephalus

0 references

heterogeneity

1 reference

based on heuristic

inferred from title

author

Stanislas Lyonnet

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1396913

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1396913%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 September 2019

Anastella Pelet

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1396913

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1396913%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 September 2019

author name string

F Serville

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1396913

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1396913%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 September 2019

M Reynaud

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1396913

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1396913%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 September 2019

C Louail

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1396913

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1396913%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 September 2019

A Munnich

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1396913

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1396913%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 September 2019

M Le Merrer

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1396913

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1396913%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 September 2019

publication date

1 July 1992

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1396913

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1396913%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 September 2019

published in

European Journal of Pediatrics

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1396913

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1396913%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 September 2019

volume

151

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1396913

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1396913%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 September 2019

issue

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1396913

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1396913%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 September 2019

page(s)

515-518

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1396913

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1396913%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 September 2019

cites work

Aqueductal Stenosis in X-Linked Hydrocephalus: a Secondary Phenomenon?

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1396913

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The syndrome of sex-linked hydrocephalus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1396913

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked aqueductal stenosis: clinical and neuropathological findings in two families

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1396913

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MASA syndrome: new clinical features and linkage analysis using DNA probes

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1396913

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MASA syndrome: further clinical delineation and chromosomal localisation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1396913

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage studies of X-linked recessive spastic paraplegia using DNA probes.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1396913

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X linked hydrocephalus: a survey of a 20 year period in Victoria, Australia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1396913

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mental retardation-clasped thumb syndrome.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1396913

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The MASA syndrome: a new heritable mental retardation syndrome

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1396913

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked hydrocephalus. Further observations

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1396913

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of X-linked hydrocephalus to Xq28 by linkage analysis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1396913

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked hydrocephalus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1396913

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic screening for hemophilia A (classic hemophilia) with a polymorphic DNA probe

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1396913

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1396913

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary stenosis of the aqueduct of Sylvius as a cause of congenital hydrocephalus

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1396913

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked mental retardation associated with bilateral clasp thumb anomaly.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1396913

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X-linked recessive aqueductal stenosis without macrocephaly

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1396913

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF01957757

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1396913

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1396913%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 September 2019

PubMed publication ID

1396913

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1396913

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1396913%20AND%20SRC:MED&resulttype=core&format=json

retrieved

15 September 2019

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q48463221&oldid=2209492465"