- Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autismZ Talebizadeh
J Med Genet 43:e21. 2006..To screen cDNA for NLGN3 and NLGN4 from lymphoblastoid cells from autistic subjects...
- Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing lossZ 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...
- No association between HOXA1 and HOXB1 genes and autism spectrum disorders (ASD)Z Talebizadeh
J Med Genet 39:e70. 2002
- Brief report: non-random X chromosome inactivation in females with autismZ 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...