Clinical experience with multiplex ligation-dependent probe amplification for microdeletion syndromes in prenatal diagnosis: 7522 pregnant Korean women

BACKGROUND: Conventional cytogenetic analysis using G-band karyotyping has been the method of choice for prenatal diagnosis, accurately detecting chromosomal abnormalities larger than 5 Mb. However, the method is inefficient for detecting the submicroscopic deletions and duplications that are associ...

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Detalhes bibliográficos
Publicado no:Mol Cytogenet
Main Authors: Lee, Dongsook, Na, Sohyun, Park, Surim, Go, Sanghee, Ma, Jinyoung, Yang, Soonha, Kim, Kichul, Lee, Seunggwan, Hwang, Doyeong
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2019
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6390335/
https://ncbi.nlm.nih.gov/pubmed/30891099
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-019-0422-8
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