A rapid and accurate methylation‐sensitive high‐resolution melting analysis assay for the diagnosis of Prader Willi and Angelman patients

Author:

Ribeiro Ferreira Igor1,Darleans dos Santos Cunha Wilton1,Henrique Ferreira Gomes Leonardo1,Azevedo Cintra Hiago1,Lopes Cabral Guimarães Fonseca Letícia2,Ferreira Bastos Elenice2,Clinton Llerena Jr. Juan2,Farias Meira de Vasconcelos Zilton1,Cunha Guida Letícia1

Affiliation:

1. Laboratório de Alta Complexidade Instituto Nacional da Saúde da Mulherda Criança e do Adolescente Fernandes FigueiraFiocruz Rio de Janeiro Brazil

2. Departamento de Genética Instituto Nacional da Saúde da Mulherda Criança e do Adolescente Fernandes FigueiraFiocruz Rio de Janeiro Brazil

Funder

Conselho Nacional de Desenvolvimento Científico e Tecnológico

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Reference44 articles.

1. Validation of a multiplex methylation‐sensitive PCR assay for the diagnosis of Prader‐Willi and Angelman's syndromes;Buller A.;Molecular Diagnosis,2000

2. Prader–Willi syndrome;Cassidy SB;European Journal of Human Genetics,2009

3. Prader‐Willi and Angelman syndromes;Cassidy S. B.;Disorders of genomic imprinting. Medicine,1998

4. A comparison of high‐resolution melting analysis with denaturing high‐performance liquid chromatography for mutation scanning: Cystic fibrosis transmembrane conductance regulator gene as a model;Chou L.‐S.;American Journal of Clinical Pathology,2005

5. High sensitivity mapping of methylated cytosines;Clark S. J.;Nucleic Acids Research,1994

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