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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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Détails bibliographiques
Auteurs principaux: Halder, Ashutosh, Jain, Manish, Chaudhary, Isha, Gupta, Neerja, Kabra, Madhulika
Format: Artigo
Langue:Inglês
Publié: Medknow Publications & Media Pvt Ltd 2013
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Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3767260/
https://ncbi.nlm.nih.gov/pubmed/24056568
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