Relevance of Copy Number Variation at Chromosome X in Male Fetuses Inherited from the Mother May Be Ascertained by Including Male Relatives from the Maternal Lineage in Addition to Trio Analyses

Chromosome microarray analysis has been used for prenatal detection of copy number variations (CNVs) and genetic counseling of CNVs has been greatly improved after the accumulation of knowledge from postnatal outcomes in terms of the genotype-phenotype correlation. However, a significant number of C...

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Detalles Bibliográficos
Autores principales: Chen, Ming, Wu, Wan-Ju, Lee, Mei-Hui, Ku, Tien-Hsiung, Ma, Gwo-Chin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564499/
https://www.ncbi.nlm.nih.gov/pubmed/32842633
http://dx.doi.org/10.3390/genes11090979

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7564499/
https://www.ncbi.nlm.nih.gov/pubmed/32842633
http://dx.doi.org/10.3390/genes11090979

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