A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family

Eitemau Tebyg

• A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family
  gan: Alasti, Fatemeh, et al.
  Cyhoeddwyd: (2008)
• A Novel Deletion Mutation in ASPM Gene in an Iranian Family with Autosomal Recessive Primary Microcephaly
  gan: AKBARIAZAR, Elinaz, et al.
  Cyhoeddwyd: (2013)
• Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss
  gan: Tabatabaiefar, MA, et al.
  Cyhoeddwyd: (2011)
• Investigating Seven Recently Identified Genes in 100 Iranian Families with Autosomal Recessive Non-syndromic Hearing Loss
  gan: Reihaneh Alikhani, et al.
  Cyhoeddwyd: (2015-09-01)
• Investigation of LRTOMT gene (locus DFNB63) mutations in Iranian patients with autosomal recessive non-syndromic hearing loss
  gan: Taghizadeh, Seyyed Hossein, et al.
  Cyhoeddwyd: (2013)