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OBSL1 gene

Known as: KIAA0657, OBSCURIN-LIKE 1, OBSL1 
 
National Institutes of Health

Papers overview

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2019
2019
3M syndrome is characterized by severe pre- and postnatal growth retardation, typical facial features, and normal intelligence… Expand
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2014
2014
CUL7, OBSL1, and CCDC8 genes are mutated in a mutually exclusive manner in 3M and other growth retardation syndromes. The… Expand
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2012
2012
3-M syndrome is a primordial growth disorder caused by mutations in CUL7, OBSL1 or CCDC8. 3-M patients typically have a modest… Expand
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Review
2012
Review
2012
3-M syndrome is an autosomal recessive primordial growth disorder characterized by small birth size and post-natal growth… Expand
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Highly Cited
2011
Highly Cited
2011
3-M syndrome, a primordial growth disorder, is associated with mutations in CUL7 and OBSL1. Exome sequencing now identifies… Expand
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Highly Cited
2011
Highly Cited
2011
The elaboration of dendrites in neurons requires secretory trafficking through the Golgi apparatus, but the mechanisms that… Expand
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2011
2011
3M syndrome (MIM 273750) is an autosomal recessive disorder characterized by pre- and post-natal growth retardation (<-4 SD… Expand
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Review
2011
Review
2011
3-M syndrome is an autosomal recessive primordial growth disorder characterised by severe postnatal growth restriction caused by… Expand
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2010
2010
3-M syndrome is an autosomal recessive disorder characterized by severe pre- and postnatal growth retardation and minor skeletal… Expand
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2009
2009
3-M syndrome is an autosomal-recessive primordial growth disorder characterized by significant intrauterine and postnatal growth… Expand
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