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Andrew J Makoff

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Genome Biology|June 19, 2007
Detailed analysis of 15q11-q14 sequence corrects errors and gaps in the public access sequence to fully reveal large segmental duplications at breakpoints for Prader-Willi, Angelman, and inv dup(15) syndromesAndrew J Makoff, Rachel H Flomen
Biological Psychiatry|September 15, 2004
The -1438A/G polymorphism in the 5-hydroxytryptamine type 2A receptor gene affects promoter activityMichael J Parsons, Ursula M D'Souza, Maria-Jesus Arranz, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 11, 2006
Association study of CHRFAM7A copy number and 2 bp deletion polymorphisms with schizophrenia and bipolar affective disorderRachel H Flomen, David A Collier, Sarah Osborne, et al.
European Journal of Human Genetics : EJHG|June 12, 2008
The copy number variant involving part of the alpha7 nicotinic receptor gene contains a polymorphic inversionRachel H Flomen, Angela F Davies, Marta Di Forti, et al.
European Journal of Human Genetics : EJHG|December 4, 2002
Haplotype and linkage disequilibrium analysis to characterise a region in the calcium channel gene CACNA1A associated with idiopathic generalised epilepsyBarry Chioza, Abena Osei-Lah, Lina Nashef, et al.
European Journal of Human Genetics : EJHG|May 17, 2012
Association between the 2-bp deletion polymorphism in the duplicated version of the alpha7 nicotinic receptor gene and P50 sensory gatingRachel H Flomen, Madiha Shaikh, Muriel Walshe, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Genome Biology|June 19, 2007
Detailed analysis of 15q11-q14 sequence corrects errors and gaps in the public access sequence to fully reveal large segmental duplications at breakpoints for Prader-Willi, Angelman, and inv dup(15) syndromesAndrew J Makoff, Rachel H Flomen
Biological Psychiatry|September 15, 2004
The -1438A/G polymorphism in the 5-hydroxytryptamine type 2A receptor gene affects promoter activityMichael J Parsons, Ursula M D'Souza, Maria-Jesus Arranz, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 11, 2006
Association study of CHRFAM7A copy number and 2 bp deletion polymorphisms with schizophrenia and bipolar affective disorderRachel H Flomen, David A Collier, Sarah Osborne, et al.
European Journal of Human Genetics : EJHG|June 12, 2008
The copy number variant involving part of the alpha7 nicotinic receptor gene contains a polymorphic inversionRachel H Flomen, Angela F Davies, Marta Di Forti, et al.
European Journal of Human Genetics : EJHG|December 4, 2002
Haplotype and linkage disequilibrium analysis to characterise a region in the calcium channel gene CACNA1A associated with idiopathic generalised epilepsyBarry Chioza, Abena Osei-Lah, Lina Nashef, et al.
European Journal of Human Genetics : EJHG|May 17, 2012
Association between the 2-bp deletion polymorphism in the duplicated version of the alpha7 nicotinic receptor gene and P50 sensory gatingRachel H Flomen, Madiha Shaikh, Muriel Walshe, et al.
Pageof 1