Extended mutational analyses of FGFR1 in osteoglop...[Am J Med Genet A. 2006] - PubMed Result

SearchDatabase nameforSearch term

Advanced Search

Your browser version may not work well with NCBI's Web applications. More information here...

Display Show

All: 1

Review: 0

Click to change filter selection through MyNCBI.

1: Am J Med Genet A. 2006 Mar 1;140(5):537-9. Links

Extended mutational analyses of FGFR1 in osteoglophonic dysplasia.

Farrow EG, Davis SI, Mooney SD, Beighton P, Mascarenhas L, Gutierrez YR, Pitukcheewanont P, White KE.

PMID: 16470795 [PubMed - indexed for MEDLINE]

Related articles

Mutations that cause osteoglophonic dysplasia define novel roles for FGFR1 in bone elongation.
Am J Hum Genet. 2005 Feb; 76(2):361-7. Epub 2004 Dec 28.

[Am J Hum Genet. 2005]
Mutation screening in patients with syndromic craniosynostoses indicates that a limited number of recurrent FGFR2 mutations accounts for severe forms of Pfeiffer syndrome.
Eur J Hum Genet. 2006 Mar; 14(3):289-98.

[Eur J Hum Genet. 2006]
[Bone dysplasia, craniosynostoses, and fibroblast growth factor receptors]
Gac Med Mex. 1995 May-Jun; 131(3):357-8.

[Gac Med Mex. 1995]
ReviewSkeletal disorders associated with fibroblast growth factor receptor mutations.
Curr Opin Genet Dev. 1997 Jun; 7(3):378-85.

[Curr Opin Genet Dev. 1997]
ReviewFinding genes involved in human developmental disorders.
Curr Opin Genet Dev. 1995 Jun; 5(3):354-61.

[Curr Opin Genet Dev. 1995]
» See reviews... | » See all...

Recent Activity

Clear Turn Off Turn On

Extended mutational analyses of FGFR1 in osteoglophonic dysplasia.Extended mutational analyses of FGFR1 in osteoglophonic dysplasia.

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Display Show