Extended mutational analyses ofFGFR1 in osteoglophonic dysplasia-Reference-Cited by-同舟云学术

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Extended mutational analyses ofFGFR1 in osteoglophonic dysplasia

Published:2006 Issue:5 Volume:140A Page:537-539
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Farrow Emily G.,Davis Siobhan I.,Mooney Sean D.,Beighton Peter,Mascarenhas Leo,Gutierrez Yvonne R.,Pitukcheewanont Pisit,White Kenneth E.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference18 articles.

1. Differential Activation of Cysteine-Substitution Mutants of Fibroblast Growth Factor Receptor 3 Is Determined by Cysteine Localization

2. Osteoglophonic dysplasia.

3. Osteoglophonic dwarfism

4. Gly369Cys mutation in mouse FGFR3 causes achondroplasia by affecting both chondrogenesis and osteogenesis

5. 2004. FGFs/FGFRs and associated disorders. In: , , editors. From inborn errors of development. New York: Oxford. Chapter 33. p 380–400.

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3. Abnormal eruption of teeth in relation to FGFR1 heterozygote mutation: a rare case of osteoglophonic dysplasia with 4-year follow-up;BMC Oral Health;2022-02-11

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