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FGD1 gene

Known as: FGD1, FYVE, RhoGEF and PH domain containing 1, ZFYVE3 
 
National Institutes of Health

Papers overview

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2017
2017
Aarskog-Scott syndrome (ASS) is a rare, X-linked recessive inherited disorder. Affected individuals may develop short stature and… Expand
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2015
2015
Aarskog–Scott syndrome (AAS), also known as faciogenital dysplasia (FGD, OMIM # 305400), is an X‐linked disorder of recessive… Expand
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2014
2014
Aarskog syndrome (AAS) is an X-linked human disease that affects the skeletal formation and embryonic morphogenesis and is caused… Expand
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2013
2013
Aarskog–Scott syndrome (ASS) is a rare disorder with characteristic facial, skeletal, and genital abnormalities. Mutations in the… Expand
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2013
2013
Frequent somatic mutations in the GNA11, matrix metalloproteinase (MMP)27, FGD1, TRRAP and GRM3 genes have been reported in… Expand
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2010
2010
Mutations in the FGD1 gene have been shown to cause Aarskog–Scott syndrome (AAS), or facio‐digito‐genital dysplasia (OMIM#305400… Expand
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2005
2005
Mutations of the FGD1 gene are responsible for a significant proportion of patients with Aarskog–Scott syndrome (AAS), an X… Expand
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Review
2004
Review
2004
Faciogenital dysplasia or Aarskog–Scott syndrome (AAS) is a genetically heterogeneous developmental disorder. The X-linked form… Expand
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2000
2000
Aarskog–Scott Syndrome (AAS) is an X‐linked disorder characterised by short stature and multiple facial, limb and genital… Expand
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Highly Cited
1998
Highly Cited
1998
We purified from rat brain a novel F-actin-binding protein with a M r of about 105,000 (p105), which was estimated by SDS… Expand
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