Methylation-Specific Multiplex Ligation-Dependent Probe Amplification Analysis of Subjects with Chromosome 15 Abnormalities

Eitemau Tebyg

• Expression of 4 Genes Between Chromosome 15 Breakpoints 1 and 2 and Behavioral Outcomes in Prader-Willi Syndrome
  gan: Bittel, Douglas C., et al.
  Cyhoeddwyd: (2006)
• Methylation-Specific Multiplex Ligation-Dependent Probe Amplification and Identification of Deletion Genetic Subtypes in Prader-Willi Syndrome
  gan: Henkhaus, Rebecca S., et al.
  Cyhoeddwyd: (2012)
• Application of Chromosomal Microarray and Multiplex Ligation-dependent Probe Amplification in prenatal diagnosis
  gan: Sharma, Pankaj, et al.
  Cyhoeddwyd: (2014)
• Multiplex ligation-dependent probe amplification workflow for the detection of submicroscopic chromosomal abnormalities in patients with developmental delay/intellectual disability
  gan: Pohovski, Leona Morozin, et al.
  Cyhoeddwyd: (2013)
• Whole genome microarray analysis of gene expression in subjects with fragile X syndrome
  gan: Bittel, Douglas C., et al.
  Cyhoeddwyd: (2007)