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Biomed Research International|June 25, 2015
DNA Methylation Levels of Melanoma Risk Genes Are Associated with Clinical Characteristics of Melanoma PatientsÉrica S S de Araújo, Dimitrius T Pramio, André Y Kashiwabara, et al.
Human Mutation|September 9, 2020
Cytogenetically visible inversions are formed by multiple molecular mechanismsMaria Pettersson, Christopher M Grochowski, Josephine Wincent, et al.
American Journal of Medical Genetics. Part A|November 15, 2015
Craniosynostosis in 10q26 deletion patients: A consequence of brain underdevelopment or altered suture biology?Ágatha Cristhina Faria, Eliete Rabbi-Bortolini, Maria R G O Rebouças, et al.
Hormone Research in Paediatrics|November 14, 2017
Recurrent Copy Number Variants Associated with Syndromic Short Stature of Unknown CauseThais K Homma, Ana C V Krepischi, Tatiane K Furuya, et al.
Plos One|January 25, 2017
Integrative Variation Analysis Reveals that a Complex Genotype May Specify Phenotype in Siblings with Syndromic Autism Spectrum DisorderViviane Neri de Souza Reis, João Paulo Kitajima, Ana Carolina Tahira, et al.
Breast Cancer Research : BCR|February 9, 2012
Germline DNA copy number variation in familial and early-onset breast cancerAna Cv Krepischi, Maria Isabel W Achatz, Erika Mm Santos, et al.
American Journal of Medical Genetics. Part A|September 29, 2011
Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridizationÉrika L Freitas, Susan M Gribble, Milena Simioni, et al.
Clinical Genetics|August 3, 2021
Congenital limb deficiency: Genetic investigation of 44 individuals presenting mainly longitudinal defects in isolated or syndromic formsLetícia Alves da Rocha, Lucas Vieira Lacerda Pires, Guilherme Lopes Yamamoto, et al.
Experimental and Molecular Pathology|September 20, 2014
Genome-wide DNA methylation profile of leukocytes from melanoma patients with and without CDKN2A mutationsÉrica Sara Souza de Araújo, Fabio Albuquerque Marchi, Tatiane Cristina Rodrigues, et al.
Nature Chemical Biology|December 12, 2018
Mechanistic insights revealed by a UBE2A mutation linked to intellectual disabilityJuliana Ferreira de Oliveira, Paula Favoretti Vital do Prado, Silvia Souza da Costa, et al.
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