Identification of Novel Microsatellite Markers Flanking the SMN1 and SMN2 Duplicated Region and Inclusion Into a Single-Tube Tridecaplex Panel for Haplotype-Based Preimplantation Genetic Testing of Spinal Muscular Atrophy

Lignende værker

• Identification of Novel Microsatellite Markers Flanking the SMN1 and SMN2 Duplicated Region and Inclusion Into a Single-Tube Tridecaplex Panel for Haplotype-Based Preimplantation Genetic Testing of Spinal Muscular Atrophy
  af: Mingjue Zhao, et al.
  Udgivet: (2019-11-01)
• Robust Preimplantation Genetic Testing of Huntington Disease by Combined Triplet-Primed PCR Analysis of the HTT CAG Repeat and Multi-Microsatellite Haplotyping
  af: Zhao, Mingjue, et al.
  Udgivet: (2019)
• SMN1 Duplications Are Associated With Progressive Muscular Atrophy, but Not With Multifocal Motor Neuropathy and Primary Lateral Sclerosis
  af: Bos, Jeroen W., et al.
  Udgivet: (2021)
• FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome
  af: Rajan-Babu, Indhu-Shree, et al.
  Udgivet: (2017)
• SMN-inducing compounds for the treatment of spinal muscular atrophy
  af: Lorson, Monique A, et al.
  Udgivet: (2012)