Prenatal diagnosis of Tay-Sachs disease: our institutional experience

Eitemau Tebyg

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