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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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Detalhes bibliográficos
Main Authors: Halder, Ashutosh, Jain, Manish, Chaudhary, Isha, Gupta, Neerja, Kabra, Madhulika
Formato: Artigo
Idioma:Inglês
Publicado em: Medknow Publications & Media Pvt Ltd 2013
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3767260/
https://ncbi.nlm.nih.gov/pubmed/24056568
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