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Sleep Medicine
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March 10, 2023
The effect of brain-derived neurotrophic factor Val66Met polymorphism on adolescent activity and rest rhythms, circadian preferences and attentional performance
Luísa da Costa Lopes, Dalva Lucia Rollemberg Poyares, Sergio Tufik, et al.
Genetics in Medicine Open
|
May 28, 2026
Unravelling ring chromosome structures and formation mechanisms by short-read and long-read genomic sequencing
Mei Ling Chong, Bruna Burssed, Chen Zhao, et al.
Genes
|
February 24, 2024
Variants in <i>KMT2A</i> in Three Individuals with Previous Suspicion of 22q11.2 Deletion Syndrome
Henrique Garcia Silveira, Carlos Eduardo Steiner, Giovana Toccoli, et al.
European Journal of Medical Genetics
|
September 15, 2010
Cytogenetic molecular delineation of a terminal 18q deletion suggesting neo-telomere formation
Leslie Domenici Kulikowski, Maisa Yoshimoto, Fernanda Teixeira da Silva Bellucco, et al.
Human Genetics
|
January 11, 2019
Downregulation of genes outside the deleted region in individuals with 22q11.2 deletion syndrome
Anelisa Gollo Dantas, Marcos Leite Santoro, Natalia Nunes, et al.
CNS Spectrums
|
June 7, 2013
Is there an association between cortical thickness, age of onset, and duration of illness in schizophrenia?
Idaiane Batista Assunção Leme, Ary Gadelha, João Ricardo Sato, et al.
Schizophrenia Research
|
June 5, 2014
Effect of antipsychotic drugs on gene expression in the prefrontal cortex and nucleus accumbens in the spontaneously hypertensive rat (SHR)
Marcos Leite Santoro, Vanessa Kiyomi Ota, Roberta Sessa Stilhano, et al.
BMC Ophthalmology
|
October 14, 2025
Ophthalmological findings in Brazilian Cornelia de Lange syndrome patients with NIPBL variants
Thainá Vilella, Beatriz Carvalho Nunes, Giulia Steuernagel Del Valle, et al.
Pediatric Cardiology
|
September 18, 2010
Investigating 22q11.2 deletion and other chromosomal aberrations in fetuses with heart defects detected by prenatal echocardiography
Fernanda Teixeira da Silva Bellucco, Sintia Iole Nogueira Belangero, Leila Montenegro Silveira Farah, et al.
American Journal of Medical Genetics. Part A
|
October 28, 2010
Cytogenetic and molecular evaluation and 20-year follow-up of a patient with ring chromosome 14
Roberta Santos Guilherme, Vera de Freitas Ayres Meloni, Claudete Palmer Sodré, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 86) with videos related to
Sort By:
Page
of 9
Sleep Medicine
|
March 10, 2023
The effect of brain-derived neurotrophic factor Val66Met polymorphism on adolescent activity and rest rhythms, circadian preferences and attentional performance
Luísa da Costa Lopes, Dalva Lucia Rollemberg Poyares, Sergio Tufik, et al.
Genetics in Medicine Open
|
May 28, 2026
Unravelling ring chromosome structures and formation mechanisms by short-read and long-read genomic sequencing
Mei Ling Chong, Bruna Burssed, Chen Zhao, et al.
Genes
|
February 24, 2024
Variants in <i>KMT2A</i> in Three Individuals with Previous Suspicion of 22q11.2 Deletion Syndrome
Henrique Garcia Silveira, Carlos Eduardo Steiner, Giovana Toccoli, et al.
European Journal of Medical Genetics
|
September 15, 2010
Cytogenetic molecular delineation of a terminal 18q deletion suggesting neo-telomere formation
Leslie Domenici Kulikowski, Maisa Yoshimoto, Fernanda Teixeira da Silva Bellucco, et al.
Human Genetics
|
January 11, 2019
Downregulation of genes outside the deleted region in individuals with 22q11.2 deletion syndrome
Anelisa Gollo Dantas, Marcos Leite Santoro, Natalia Nunes, et al.
CNS Spectrums
|
June 7, 2013
Is there an association between cortical thickness, age of onset, and duration of illness in schizophrenia?
Idaiane Batista Assunção Leme, Ary Gadelha, João Ricardo Sato, et al.
Schizophrenia Research
|
June 5, 2014
Effect of antipsychotic drugs on gene expression in the prefrontal cortex and nucleus accumbens in the spontaneously hypertensive rat (SHR)
Marcos Leite Santoro, Vanessa Kiyomi Ota, Roberta Sessa Stilhano, et al.
BMC Ophthalmology
|
October 14, 2025
Ophthalmological findings in Brazilian Cornelia de Lange syndrome patients with NIPBL variants
Thainá Vilella, Beatriz Carvalho Nunes, Giulia Steuernagel Del Valle, et al.
Pediatric Cardiology
|
September 18, 2010
Investigating 22q11.2 deletion and other chromosomal aberrations in fetuses with heart defects detected by prenatal echocardiography
Fernanda Teixeira da Silva Bellucco, Sintia Iole Nogueira Belangero, Leila Montenegro Silveira Farah, et al.
American Journal of Medical Genetics. Part A
|
October 28, 2010
Cytogenetic and molecular evaluation and 20-year follow-up of a patient with ring chromosome 14
Roberta Santos Guilherme, Vera de Freitas Ayres Meloni, Claudete Palmer Sodré, et al.
Page
of 9