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pro vyhledávání: '"Laiara Cristina de Souza"'
Autor:
Laiara Cristina de Souza, Vera Lúcia Gil-da-Silva-Lopes, Ilária Cristina Sgardioli, Társis Paiva Vieira
Publikováno v:
American Journal of Medical Genetics Part A. 176:1753-1759
Submicroscopic deletions in chromosome 19 have been rarely reported. We reported a male patient presenting with neurodevelopmental delay and facial dysmorphisms with a de novo 19p13.11p13.12 deletion of approximately 1.4 Mb. To date, there are seven
Autor:
Laiara Cristina de Souza
Publikováno v:
Biblioteca Digital de Teses e Dissertações da Universidade Estadual de Campinas (UNICAMP)
Universidade Estadual de Campinas (UNICAMP)
instacron:UNICAMP
Universidade Estadual de Campinas (UNICAMP)
instacron:UNICAMP
Orientadores: Társis Antonio Paiva Vieira; Vera Lúcia Gil da Silva Lopes Dissertação (mestrado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas Resumo: Em 2010, The International Standards for Cytogenomic Array (ISCA) Consort
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30792fcfbdf052080988e2a9cecb80e7
Autor:
Laiara Cristina de Souza, Matheus de Mello Copelli, Miriam Coelho Molck, Társis Paiva Vieira, Ilária Cristina Sgardioli, Ana Paula Santos, Amanda Sodré Bioto
Publikováno v:
Anais do Congresso de Iniciação Científica da Unicamp.
Autor:
Laiara Cristina de Souza, Vera Lúcia Gil da Silva Lopes, Ilária Cristina Sgardioli, Társis Paiva Vieira
Publikováno v:
Semina: Ciências Biológicas e da Saúde. 38:63
Submicroscopic deletions in chromosome 19 have been rarely reported. The aim of this study was to describe the genotype-phenotype correlation of a 19p13.11-p13.12 deletion . A male patient was referred for genetic evaluation by presenting neurodevelo