Cloning and regional localization of the mouse faciogenital dysplasia (Fgd1) gene (Q48070907)

From Wikidata

Jump to navigation Jump to search

scientific article

Language	Label	Description	Also known as
English	Cloning and regional localization of the mouse faciogenital dysplasia (Fgd1) gene	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8535076

Cloning and regional localization of the mouse faciogenital dysplasia (Fgd1) gene (English)

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8535076

author name string

N G Pasteris

1

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8535076

B de Gouyon

2

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8535076

A B Cadle

3

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8535076

K Campbell

4

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8535076

G E Herman

5

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8535076

J L Gorski

6

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8535076

publication date

1 September 1995

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8535076

number of pages

4

1 reference

based on heuristic

inferred from page(s)

Mammalian Genome

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8535076

6

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8535076

9

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8535076

658-661

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8535076

https://scigraph.springernature.com/pub.10.1007/bf00352375

0 references

Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X chromosome: implications for mapping human disorders in Xq28

1 reference

https://pubmed.ncbi.nlm.nih.gov/8535076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factor

1 reference

https://pubmed.ncbi.nlm.nih.gov/8535076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic linkage of the erythroid-specific delta-aminolevulinate synthase gene (Alas2) to the distal region of the mouse X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8535076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New insights into the man-mouse comparative map of the X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8535076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aarskog syndrome: full male and female expression associated with an X-autosome translocation

1 reference

https://pubmed.ncbi.nlm.nih.gov/8535076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Close linkage of the murine locus bare patches to the X-linked visual pigment gene: implications for mapping human X-linked dominant chondrodysplasia punctata

1 reference

https://pubmed.ncbi.nlm.nih.gov/8535076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A comprehensive set of sequence analysis programs for the VAX

1 reference

https://pubmed.ncbi.nlm.nih.gov/8535076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Proteins regulating Ras and its relatives

1 reference

https://pubmed.ncbi.nlm.nih.gov/8535076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aarskog syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8535076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A radiation hybrid map of the proximal short arm of the human X chromosome spanning incontinentia pigmenti 1 (IP1) translocation breakpoints

1 reference

https://pubmed.ncbi.nlm.nih.gov/8535076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xp11.2-Xq13).

1 reference

https://pubmed.ncbi.nlm.nih.gov/8535076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mouse X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8535076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Translocation breakpoint in Aarskog syndrome maps to Xp11.21 between ALAS2 and DXS323

1 reference

https://pubmed.ncbi.nlm.nih.gov/8535076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Aarskog-Scott syndrome: confirmation of linkage to the pericentromeric region of the X chromosome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8535076

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00352375

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8535076

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

8 February 2018

http://europepmc.org/abstract/MED/8535076

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q48070907&oldid=2183732036"