Prenatal Diagnosis by Chromosome Microarray Analysis, An Indian Experience

BACKGROUND: Karyotyping has been the gold standard for prenatal chromosome analysis. The resolution should be higher by chromosome microarray analysis (CMA). The challenge lies in recognizing benign and pathogenic or clinically significant copy number variations (pCNV) and variations of unknown sign...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:J Obstet Gynaecol India
Main Authors: Bajaj Lall, Meena, Agarwal, Shruti, Paliwal, Preeti, Saviour, Pushpa, Joshi, Anju, Joshi, Arti, Mahajan, Surbhi, Bijarnia-Mahay, Sunita, Dua Puri, Ratna, Verma, I. C.
Formato: Artigo
Idioma:Inglês
Publicado em: Springer India 2021
Assuntos:
Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8167018/
https://ncbi.nlm.nih.gov/pubmed/34149218
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13224-020-01413-6
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados