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

Antzeko izenburuak

• A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family
  nork: Alasti, Fatemeh, et al.
  Argitaratua: (2008)
• Genetic Linkage Analysis of 15 DFNB Loci in a Group of Iranian Families with Autosomal Recessive Hearing Loss
  nork: Tabatabaiefar, MA, et al.
  Argitaratua: (2011)
• A Novel Deletion Mutation in ASPM Gene in an Iranian Family with Autosomal Recessive Primary Microcephaly
  nork: AKBARIAZAR, Elinaz, et al.
  Argitaratua: (2013)
• Investigating Seven Recently Identified Genes in 100 Iranian Families with Autosomal Recessive Non-syndromic Hearing Loss
  nork: Reihaneh Alikhani, et al.
  Argitaratua: (2015-09-01)
• Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked family
  nork: Reiisi, Somayeh, et al.
  Argitaratua: (2016)