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. (Q52605648)
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scientific article published in December 2010
| Language | Label | Description | Also known as |
|---|---|---|---|
| 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 |
Statements
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)
Katsu Takahashi
Masaki Nagata
Glen H Nuckolls
Xibin Wang
Lillian Shum
Yukie Seki
Tomoyuki Kawase
Kazuaki Nonaka
Ichiro Takahashi
Arhab A Noman
Kenji Suzuki
Harold C Slavkin
1 December 2010
48
4
847-856