Z Talebizadeh

Summary

Affiliation: Boys Town National Research Hospital
Country: USA

Publications

  1. pmc Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism
    Z Talebizadeh
    J Med Genet 43:e21. 2006
  2. ncbi request reprint Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss
    Z Talebizadeh
    Center for Hereditary Communication Disorders, Boys Town National Research Hospital, Omaha, Nebraska
    Hum Mutat 14:493-501. 1999
  3. pmc No association between HOXA1 and HOXB1 genes and autism spectrum disorders (ASD)
    Z Talebizadeh
    J Med Genet 39:e70. 2002
  4. ncbi request reprint Brief report: non-random X chromosome inactivation in females with autism
    Z Talebizadeh
    Section of Medical Genetics and Molecular Medicine, Children s Mercy Hospitals and Clinics, University of Missouri Kansas City School of Medicine, MO 64108, USA
    J Autism Dev Disord 35:675-81. 2005

Detail Information

Publications4

  1. pmc Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autism
    Z Talebizadeh
    J Med Genet 43:e21. 2006
    ..To screen cDNA for NLGN3 and NLGN4 from lymphoblastoid cells from autistic subjects...
  2. ncbi request reprint Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing loss
    Z Talebizadeh
    Center for Hereditary Communication Disorders, Boys Town National Research Hospital, Omaha, Nebraska
    Hum Mutat 14:493-501. 1999
    ..Mutation analysis of KCNQ4 was also performed on 80 unrelated probands from families with recessive or dominant nonsyndromic hearing loss. None of these cases showed a truncated mutation in KCNQ4...
  3. pmc No association between HOXA1 and HOXB1 genes and autism spectrum disorders (ASD)
    Z Talebizadeh
    J Med Genet 39:e70. 2002
  4. ncbi request reprint Brief report: non-random X chromosome inactivation in females with autism
    Z Talebizadeh
    Section of Medical Genetics and Molecular Medicine, Children s Mercy Hospitals and Clinics, University of Missouri Kansas City School of Medicine, MO 64108, USA
    J Autism Dev Disord 35:675-81. 2005
    ..X chromosome skewness has been reported in female carriers of other neurological disorders such as X-linked mental retardation, adrenoleukodystrophy and Rett syndrome...