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Cancer Research
|
October 19, 2001
A polymorphism in endostatin, an angiogenesis inhibitor, predisposes for the development of prostatic adenocarcinoma
P Iughetti, O Suzuki, P H Godoi, et al.
Clinical Genetics
|
June 29, 2016
Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss-of-function vs missense variants
C P Savastano, L A Brito, Á C Faria, et al.
Clinical Genetics
|
April 29, 2005
Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly
F S Jehee, D Johnson, L G Alonso, et al.
Brain Research
|
November 29, 2008
HTR1B and HTR2C in autism spectrum disorders in Brazilian families
G M Orabona, K Griesi-Oliveira, E Vadasz, et al.
Nature Genetics
|
September 10, 1998
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B
R Bashir, S Britton, T Strachan, 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 disorder
J R Oliveira, D R Carvalho, D Pontual, et al.
Journal of Medical Genetics
|
May 6, 2008
High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation
F S Jehee, A C V Krepischi-Santos, K M Rocha, et al.
Emerging Infectious Diseases
|
December 11, 2025
Yellow Fever Virus in Aedes albopictus Mosquitoes from Urban Green Area, São Paulo State, Brazil
Eduardo S Bergo, Juliana Telles de-Deus, Luis F Mucci, et al.
Cytogenetic and Genome Research
|
November 25, 2006
Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations
A C V Krepischi-Santos, A M Vianna-Morgante, F S Jehee, et al.
Journal of Dental Research
|
October 21, 2017
MRPL53, a New Candidate Gene for Orofacial Clefting, Identified Using an eQTL Approach
C Masotti, L A Brito, A C Nica, et al.
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of 15
Search research articles
Search
Showing results (131-140 of 142) with videos related to
Sort By:
Page
of 15
Cancer Research
|
October 19, 2001
A polymorphism in endostatin, an angiogenesis inhibitor, predisposes for the development of prostatic adenocarcinoma
P Iughetti, O Suzuki, P H Godoi, et al.
Clinical Genetics
|
June 29, 2016
Impact of rare variants in ARHGAP29 to the etiology of oral clefts: role of loss-of-function vs missense variants
C P Savastano, L A Brito, Á C Faria, et al.
Clinical Genetics
|
April 29, 2005
Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly
F S Jehee, D Johnson, L G Alonso, et al.
Brain Research
|
November 29, 2008
HTR1B and HTR2C in autism spectrum disorders in Brazilian families
G M Orabona, K Griesi-Oliveira, E Vadasz, et al.
Nature Genetics
|
September 10, 1998
A gene related to Caenorhabditis elegans spermatogenesis factor fer-1 is mutated in limb-girdle muscular dystrophy type 2B
R Bashir, S Britton, T Strachan, 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 disorder
J R Oliveira, D R Carvalho, D Pontual, et al.
Journal of Medical Genetics
|
May 6, 2008
High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation
F S Jehee, A C V Krepischi-Santos, K M Rocha, et al.
Emerging Infectious Diseases
|
December 11, 2025
Yellow Fever Virus in Aedes albopictus Mosquitoes from Urban Green Area, São Paulo State, Brazil
Eduardo S Bergo, Juliana Telles de-Deus, Luis F Mucci, et al.
Cytogenetic and Genome Research
|
November 25, 2006
Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations
A C V Krepischi-Santos, A M Vianna-Morgante, F S Jehee, et al.
Journal of Dental Research
|
October 21, 2017
MRPL53, a New Candidate Gene for Orofacial Clefting, Identified Using an eQTL Approach
C Masotti, L A Brito, A C Nica, et al.
Page
of 15