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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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Detalles Bibliográficos
Autores principales:	Lee, Dongsook, Na, Sohyun, Park, Surim, Go, Sanghee, Ma, Jinyoung, Yang, Soonha, Kim, Kichul, Lee, Seunggwan, Hwang, Doyeong
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2019
Materias:	Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390335/ https://www.ncbi.nlm.nih.gov/pubmed/30891099 http://dx.doi.org/10.1186/s13039-019-0422-8

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