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1 Klippel-Feil syndrome is a skeletal malformation charact
2 ateral absence of C1, odontoid anomalies
and Klippel-Feil syndrome.
3 Other syndromes such
as Klippel-Feil, familial dysautonomia, and Marfan syndrome
4 f VG5Q in patients with the vascular
disease Klippel-Trenaunay syndrome (KTS).
5 Aggf1 is the first gene identified
for Klippel-Trenaunay syndrome (KTS), and encodes an angioge
6 st-derived is specifically affected in
human Klippel-Feil syndrome, Sprengel's deformity and Arnold-C
7 GDF6, GDF3) implicated in the development
of Klippel-Feil syndrome (KFS).
8 with a vascular malformation consistent
with Klippel-Trenaunay syndrome (KTS).
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