Prenatal diagnosis of Tay-Sachs disease: our institutional experience

Benzer Materyaller

• Identification of novel mutations in HEXA gene in children affected with Tay-Sachs disease from India
  Yazar:: Mistri, Mehul, ve diğerleri
  Baskı/Yayın Bilgisi: (2014)
• Prenatal diagnosis of lysosomal storage disorders: our experience in 120 cases
  Yazar:: Mistri, Mehul, ve diğerleri
  Baskı/Yayın Bilgisi: (2014)
• Expanding the spectrum of HEXA mutations in Indian patients with Tay–Sachs disease
  Yazar:: Sheth, Jayesh, ve diğerleri
  Baskı/Yayın Bilgisi: (2014)
• Identification of Novel Mutations in HEXA Gene in Children Affected with Tay Sachs Disease from India
  Yazar:: Mistri, Mehul, ve diğerleri
  Baskı/Yayın Bilgisi: (2012)
• Identification of deletion-duplication in HEXA gene in five children with Tay-Sachs disease from India
  Yazar:: Sheth, Jayesh, ve diğerleri
  Baskı/Yayın Bilgisi: (2018)