Application of Chromosomal Microarray and Multiplex Ligation-dependent Probe Amplification in prenatal diagnosis

Παρόμοια τεκμήρια

• Prenatal diagnosis of steroid 21-hydroxylase-deficient congenital adrenal hyperplasia: Experience from a tertiary care centre in India
  ανά: Dubey, Sudhisha, κ.ά.
  Έκδοση: (2017)
• Inherited 5p deletion syndrome due to paternal balanced translocation: Phenotypic heterogeneity due to duplication of 8q and 12p
  ανά: Sharma, Pankaj, κ.ά.
  Έκδοση: (2013)
• Can we rely on the multiplex ligation-dependent probe amplification method (MLPA) for prenatal diagnosis?
  ανά: Omrani, Mir Davood, κ.ά.
  Έκδοση: (2014)
• AB095. Prenatal diagnosis of Duchenne muscular dystrophy by combining of multiplex Polymerase Chain Reaction and Multiplex Ligation dependent Probe Amplification
  ανά: Ngo, Manh Tien, κ.ά.
  Έκδοση: (2017)
• Multiplex ligation-dependent probe amplification versus karyotyping in prenatal diagnosis: the M.A.K.E. study
  ανά: Boormans, Elisabeth MA, κ.ά.
  Έκδοση: (2008)