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

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

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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

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

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