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Copy number imbalances detected with a BAC-based array comparative genomic hybridization platform in congenital diaphragmatic hernia fetuses
(Funpec-editoraRibeirao PretoBrasil, 2011)
Genomic Profile Of The Sarcomatoid Ex-pleomorphic Adenoma By Array Comparative Genomic Hybridization
(AMER SOC CLINICAL PATHOLOGYCHICAGO, 2015)
Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH)
(Elsevier B.V., 2016-03-01)
Autism spectrum disorder (ASD) has a strong genetic basis and advances in genomic scanning methods have resulted in the identification of the underlying alterations in about 30% of the cases. The overwhelming majority of ...
Genomic imbalances detected through array CGH in fetuses with holoprosencephalyInstabilidades genômicas detectadas através de array CGH em fetos com holoprosencefalia
(Academia Brasileira de Neurologia - ABNEURO, 2011)
Genomic and phenotypic profiles of two Brazilian breast cancer cell lines derived from primary human tumors
(2013-04-01)
Breast cancer is the most common type of cancer among women worldwide. Research using breast cancer cell lines derived from primary tumors may provide valuable additional knowledge regarding this type of cancer. Therefore, ...
Genomic and phenotypic profiles of two Brazilian breast cancer cell lines derived from primary human tumors
(2013-04-01)
Breast cancer is the most common type of cancer among women worldwide. Research using breast cancer cell lines derived from primary tumors may provide valuable additional knowledge regarding this type of cancer. Therefore, ...