Wikidata

(Q52605648)

English

The primary site of the acrocephalic feature in Apert Syndrome is a dwarf cranial base with accelerated chondrocytic differentiation due to aberrant activation of the FGFR2 signaling.

scientific article published in December 2010

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Statements

title
The primary site of the acrocephalic feature in Apert Syndrome is a dwarf cranial base with accelerated chondrocytic differentiation due to aberrant activation of the FGFR2 signaling. (English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
21129456
retrieved
4 May 2018
reference URL
http://europepmc.org/abstract/MED/21129456
author name string

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