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FG SYNDROME 2

Known as: FGS2 
National Institutes of Health

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FG syndrome

Papers overview

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2012
2012
FG syndrome: The FGS2 locus revisited
FG Syndrome: The FGS2 Locus Revisited Olivier Perche, B eatrice Laudier, Arnaud Menuet, Sylvie Odent, Frederic Laumonnier, and… 
2009
2009
An examination of anatomic, physiologic, and metabolic factors associated with well-being of broilers differing in field gait score.
An experiment was conducted to evaluate potential differences for indicators of well-being in birds classified as having field… 
Highly Cited
2007
Highly Cited
2007
Filamin A mutation is one cause of FG syndrome
FG syndrome was originally described as a rare syndromic cause of X‐linked mental retardation associated with congenital heart… 
2003
2003
Genetic heterogeneity of FG syndrome: a fourth locus (FGS4) maps to Xp11.4-p11.3 in an Italian family
Abstract. FG syndrome (FGS, MIM 305450) is a rare X-linked recessive disorder comprising mental retardation and multiple… 
2000
2000
Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: a second FG locus [FGS2]?
FG syndrome is an X-linked condition comprising mental retardation, congenital hypotonia, macrocephaly, distinctive facial… 
1997
1997
On-Orbit Test of Clearing Slews in FGS2 Star Selector Servo A
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