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HYLS1 gene

Known as: FLJ32915, HYLS1, hydrolethalus syndrome 1 
National Institutes of Health

Papers overview

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2020
2020
Cilia and flagella are conserved subcellular organelles, which arise from centrioles and play critical roles in development and… Expand
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2020
2020
Abstract Woolly mammoths were among the most abundant cold-adapted species during the Pleistocene. Their once-large populations… Expand
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2016
2016
The p.Asp211Gly homozygous HYLS1 mutation is so far known to cause only hydrolethalus syndrome, a lethal malformation syndrome… Expand
2009
2009
BackgroundHydrolethalus syndrome (HLS) is a severe fetal malformation syndrome characterized by multiple developmental anomalies… Expand
2009
2009
Hydrolethalus syndrome (HLS) is a severe fetal malformation syndrome that is inherited by an autosomal recessive manner. HLS… Expand
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2008
2008
Hydrolethalus syndrome is a lethal malformation syndrome with a severe brain malformation, most often hydrocephaly and absent… Expand
2005
2005
Hydrolethalus syndrome (HLS) is an autosomal recessive lethal malformation syndrome characterized by multiple developmental… Expand
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