General comparison of CMA results correlated with routine cytogenetic results

NIAID Data Ecosystem2026-03-06 收录

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General comparison of CMA results correlated with routine cytogenetic results

创建时间：

2007-03-28

Test No. 483: Mammalian Spermatogonial Chromosomal Aberration Test

生殖细胞突变

染色体异常

This test measures structural chromosomal aberrations (both chromosome- and chromatid-type) in dividing spermatogonial germ cells and is, therefore, expected to be predictive of induction of heritable

Organisation for Economic Co-operation and Development90

Cavum septi pellucidi width in fetuses with cavum septi pellucidi-et-vergae and its association with aneuploidies

胎儿发育

染色体异常

This dataset contains data used for analysis in this paper as excel sheets. Also contains tables of statistical analysis and a few examples of images wherein the measurements were obtained.

DataCite Commons2021-04-12 更新80

Comparison of clinical outcomes from baseline analysis of the two screening approaches in a general screening population.

筛查评估

染色体异常

NIPT, non-invasive prenatal testing * 70% of total affected pregnancies (30% receive no screening). † Assuming termination rates for trisomy 21, trisomy 18, trisomy 13, and monosomy X of 87%, 81%, 90%

NIAID Data Ecosystem40

Table2_A retrospective single-center analysis of prenatal diagnosis and follow-up of 626 chinese patients with positive non-invasive prenatal screening results.doc

产前基因诊断

染色体异常

This study explored the diagnostic efficiency of different prenatal diagnostic approaches for women with positive non-invasive prenatal screening (NIPS) results by analyzing their clinical information

NIAID Data Ecosystem80

Recurrent genomic instability of chromosome 1q in neural derivatives of human embryonic stem cells. Homo sapiens

细胞基因组不稳定性

染色体异常

array-CGH analysis of human neural stem cells derived from human ES cells during long term in vitro culture Overall design: array-CGH analysis of human neural stem cells derived from human ES cells co

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General comparison of CMA results correlated with routine cytogenetic results

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