Fluorescence in situ hybridization (FISH) using non-commercial probes in the diagnosis of clinically suspected microdeletion syndromes

BACKGROUND & OBJECTIVES: Microdeletion syndromes are characterized by small (<5 Mb) chromosomal deletions in which one or more genes are involved. These are frequently associated with multiple congenital anomalies. The phenotype is the result of haploinsufficiency of genes in the critical int...

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Detalles Bibliográficos
Autores principales: Halder, Ashutosh, Jain, Manish, Chaudhary, Isha, Gupta, Neerja, Kabra, Madhulika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3767260/
https://www.ncbi.nlm.nih.gov/pubmed/24056568

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3767260/
https://www.ncbi.nlm.nih.gov/pubmed/24056568

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