Genetic Counseling for a Prenatal Diagnosis of Structural Chromosomal Abnormality with High-Resolution Analysis Using a Single Nucleotide Polymorphism Microarray

A 41-year old pregnant woman underwent amniocentesis to conduct a conventional karyotyping analysis; the analysis reported an abnormal karyotype: 46, XY, add(9)(p24). Chromosomal microarray analysis (CMA) is utilized in prenatal diagnoses. A single nucleotide polymorphism microarray revealed a male...

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Detalles Bibliográficos
Autores principales: Takashima, Akiko, Takeshita, Naoki, Kinoshita, Toshihiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications, Pavia, Italy 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5067401/
https://www.ncbi.nlm.nih.gov/pubmed/27777709
http://dx.doi.org/10.4081/cp.2016.852

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5067401/
https://www.ncbi.nlm.nih.gov/pubmed/27777709
http://dx.doi.org/10.4081/cp.2016.852

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