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Prenatal diagnosis of maternal partial trisomy 9p23p24.3 and 14q11.2q21.3 in a fetus: a case report

OBJECTIVE: This study aimed to report a fetus with maternal partial trisomy 9p and 14q and the phenotype detected in ultrasound. METHODS: The chromosome rearrangements in the fetus were characterized by G-banding and chromosome microarray analysis based on single nucleotide polymorphism (SNP) array...

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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Mol Cytogenet
Asıl Yazarlar: Wu, J. B., Sha, J., Zhai, J. F., Liu, Y., Zhang, B.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2020
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7006427/
https://ncbi.nlm.nih.gov/pubmed/32055256
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-020-0473-x
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