A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome.

Reha M Toydemir; Anna E Brassington; Pinar Bayrak-Toydemir; Patrycja A Krakowiak; Lynn B Jorde; Frank G Whitby; Nicola Longo; David H Viskochil; John C Carey; Michael J Bamshad

doi:10.1086/508433

A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome.

Identifier:nobleid.org/w1/20260515/AD62CD90

Type:Journal Article

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Reha M Toydemir

Anna E Brassington

Pinar Bayrak-Toydemir

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A novel mutation in FGFR3 causes camptodactyly, tall stature, and hearing loss (CATSHL) syndrome.

Identifier:nobleid.org/w1/20260515/AD62CD90

Type:Journal Article

0 views

Support unavailableClaim Your Authorship

View Original Paper Source

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Reha M Toydemir

Anna E Brassington

Pinar Bayrak-Toydemir

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