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Z Talebizadeh

Showing results (1-10 of 7) with videos related to

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Clinical Genetics|February 5, 2005
Insulin resistance and obesity-related factors in Prader-Willi syndrome: comparison with obese subjectsZ Talebizadeh, M G Butler
Journal of Medical Genetics|August 16, 2003
Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPDD C Bittel, N Kibiryeva, Z Talebizadeh, et al.
Journal of Autism and Developmental Disorders|September 17, 2005
Brief report: non-random X chromosome inactivation in females with autismZ Talebizadeh, D C Bittel, O J Veatch, et al.
Human Mutation|November 26, 1999
Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing lossZ Talebizadeh, P M Kelley, J W Askew, et al.
Journal of Medical Genetics|December 25, 2007
Comparison of X-chromosome inactivation patterns in multiple tissues from human femalesD C Bittel, M F Theodoro, N Kibiryeva, et al.
Journal of Medical Genetics|May 2, 2006
Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autismZ Talebizadeh, D Y Lam, M F Theodoro, et al.
Journal of Medical Genetics|April 5, 2005
Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutationsM G Butler, M J Dasouki, X-P Zhou, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Clinical Genetics|February 5, 2005
Insulin resistance and obesity-related factors in Prader-Willi syndrome: comparison with obese subjectsZ Talebizadeh, M G Butler
Journal of Medical Genetics|August 16, 2003
Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPDD C Bittel, N Kibiryeva, Z Talebizadeh, et al.
Journal of Autism and Developmental Disorders|September 17, 2005
Brief report: non-random X chromosome inactivation in females with autismZ Talebizadeh, D C Bittel, O J Veatch, et al.
Human Mutation|November 26, 1999
Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing lossZ Talebizadeh, P M Kelley, J W Askew, et al.
Journal of Medical Genetics|December 25, 2007
Comparison of X-chromosome inactivation patterns in multiple tissues from human femalesD C Bittel, M F Theodoro, N Kibiryeva, et al.
Journal of Medical Genetics|May 2, 2006
Novel splice isoforms for NLGN3 and NLGN4 with possible implications in autismZ Talebizadeh, D Y Lam, M F Theodoro, et al.
Journal of Medical Genetics|April 5, 2005
Subset of individuals with autism spectrum disorders and extreme macrocephaly associated with germline PTEN tumour suppressor gene mutationsM G Butler, M J Dasouki, X-P Zhou, et al.
Pageof 1