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Showing results (51-60 of 57) with videos related to

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Molecular Psychiatry|March 24, 1999
The association of the short variant of the 5-HTTPLR polymorphism and the apoE epsilon4 allele does not increase the risk for late onset Alzheimer's diseaseJ R Oliveira, C M Shimokomaki, P R Brito-Marques, et al.
Cytogenetic and Genome Research|July 21, 2009
Constitutional haploinsufficiency of tumor suppressor genes in mentally retarded patients with microdeletions in 17p13.1A C V Krepischi-Santos, D Rajan, I K Temple, et al.
Journal of Medical Genetics|June 28, 2005
Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parentsC Rosenberg, J Knijnenburg, E Bakker, et al.
Molecular Psychiatry|July 13, 2000
Analysis of the serotonin transporter polymorphism (5-HTTLPR) in Brazilian patients affected by dysthymia, major depression and bipolar disorderJ R Oliveira, D R Carvalho, D Pontual, et al.
Clinical Genetics|October 8, 2009
Chromosome imbalances in syndromic hearing lossA L P M Catelani, A C V Krepischi, C A Kim, et al.
Cytogenetic and Genome Research|November 25, 2006
Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterationsA C V Krepischi-Santos, A M Vianna-Morgante, F S Jehee, et al.
American Journal of Medical Genetics|April 20, 1999
Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study--preliminary dataD J Allingham-Hawkins, R Babul-Hirji, D Chitayat, et al.
Pageof 6

Showing results (51-60 of 57) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 57 results.
Molecular Psychiatry|March 24, 1999
The association of the short variant of the 5-HTTPLR polymorphism and the apoE epsilon4 allele does not increase the risk for late onset Alzheimer's diseaseJ R Oliveira, C M Shimokomaki, P R Brito-Marques, et al.
Cytogenetic and Genome Research|July 21, 2009
Constitutional haploinsufficiency of tumor suppressor genes in mentally retarded patients with microdeletions in 17p13.1A C V Krepischi-Santos, D Rajan, I K Temple, et al.
Journal of Medical Genetics|June 28, 2005
Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parentsC Rosenberg, J Knijnenburg, E Bakker, et al.
Molecular Psychiatry|July 13, 2000
Analysis of the serotonin transporter polymorphism (5-HTTLPR) in Brazilian patients affected by dysthymia, major depression and bipolar disorderJ R Oliveira, D R Carvalho, D Pontual, et al.
Clinical Genetics|October 8, 2009
Chromosome imbalances in syndromic hearing lossA L P M Catelani, A C V Krepischi, C A Kim, et al.
Cytogenetic and Genome Research|November 25, 2006
Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterationsA C V Krepischi-Santos, A M Vianna-Morgante, F S Jehee, et al.
American Journal of Medical Genetics|April 20, 1999
Fragile X premutation is a significant risk factor for premature ovarian failure: the International Collaborative POF in Fragile X study--preliminary dataD J Allingham-Hawkins, R Babul-Hirji, D Chitayat, et al.
Pageof 6