HYLS1 gene

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

Topic mentions per year

Topic mentions per year

2005-2016
0120052016

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
The p.Asp211Gly homozygous HYLS1 mutation is so far known to cause only hydrolethalus syndrome, a lethal malformation syndrome… (More)
  • figure 1
  • figure 2
  • figure 3
Is this relevant?
2011
2011
Hydrolethalus syndrome is a severe lethal disorder most commonly found in Finland. We present a lethal case of complex congenital… (More)
Is this relevant?
2009
2009
BACKGROUND Hydrolethalus syndrome (HLS) is a severe fetal malformation syndrome characterized by multiple developmental anomalies… (More)
Is this relevant?
2009
2009
Hydrolethalus syndrome (HLS) is a severe fetal malformation syndrome that is inherited by an autosomal recessive manner. HLS… (More)
  • figure 1
  • figure 2
  • figure 3
  • table 1
  • figure 4
Is this relevant?
2008
2008
Hydrolethalus syndrome is a lethal malformation syndrome with a severe brain malformation, most often hydrocephaly and absent… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
2005
2005
Hydrolethalus syndrome (HLS) is an autosomal recessive lethal malformation syndrome characterized by multiple developmental… (More)
  • figure 1
  • table 1
  • table 2
  • figure 2
  • figure 3
Is this relevant?