Does increase in genomic microarray resolution result in increased diagnostic yield? (2014)
- Autores:
- Autores USP: COSTA, SILVIA SOUZA DA - IB ; KREPISCHI, ANA CRISTINA VICTORINO - IB ; ROSENBERG, CARLA - IB
- Unidade: IB
- Assuntos: DEFICIÊNCIA MENTAL (DIAGNÓSTICO); GENÉTICA MÉDICA; EXPRESSÃO GÊNICA
- Idioma: Inglês
- Imprenta:
- Editora: American Society of Human Genetics
- Local: San Diego, CA
- Data de publicação: 2014
- Fonte:
- Título do periódico: Abstrcts
- Nome do evento: Annual Meeting of the American Society of Human Genetic (ASHG)
-
ABNT
COSTA, Sílvia S e KREPISCHI, Ana Cristina Victorino e ROSENBERG, Carla. Does increase in genomic microarray resolution result in increased diagnostic yield? 2014, Anais.. San Diego, CA: American Society of Human Genetics, 2014. . Acesso em: 25 set. 2024. -
APA
Costa, S. S., Krepischi, A. C. V., & Rosenberg, C. (2014). Does increase in genomic microarray resolution result in increased diagnostic yield? In Abstrcts. San Diego, CA: American Society of Human Genetics. -
NLM
Costa SS, Krepischi ACV, Rosenberg C. Does increase in genomic microarray resolution result in increased diagnostic yield? Abstrcts. 2014 ;[citado 2024 set. 25 ] -
Vancouver
Costa SS, Krepischi ACV, Rosenberg C. Does increase in genomic microarray resolution result in increased diagnostic yield? Abstrcts. 2014 ;[citado 2024 set. 25 ] - Molecular and cellular basis of hyperassembly and protein aggregation driven by a rare pathogenic mutation in DDX3X
- Cytogenetically visible inversions are formed by multiple molecular mechanisms
- LINE-1 hypermethylation in peripheral blood of cutaneous melanoma patients is associated with metastasis
- Rare germline copy number variations in hereditary cutaneous melanoma
- Insights in osteosarcoma by proton nuclear magnetic resonance serum metabonomics
- Efficient detection of chromosome imbalances and single nucleotide variants using targeted sequencing in the clinical setting
- Mechanistic insights revealed by a UBE2A mutation linked to intellectual disability
- Dental developmental abnormalities in a patient with subtelomeric 7q36 deletion syndrome may confirm a novel role for the SHH gene
- Lymphovascular invasion and histologic grade are associated with specific genomic profiles in invasive carcinomas of the breast
- Upregulated genes at 2q24 gains as candidate oncogenes in hepatoblastomas
Como citar
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas