Gamut of Genetic Testing for Neonatal Care

被引：5
|
作者：
Ankala, Arunkanth [1 ]
Hegde, Madhuri R. [1 ]
机构：
[1] Emory Univ, Sch Med, Dept Human Genet, Atlanta, GA 30322 USA
来源：
CLINICS IN PERINATOLOGY | 2015年 / 42卷 / 02期
关键词：
Genetic testing; Perinatal diagnostics; Clinical genetics; Neonatal diagnostics; Exome sequencing; MUTATION; DIAGNOSIS; GENOME; EXOME; ARRAY; MICRODELETION; MICROARRAY;
D O I：
10.1016/j.clp.2015.02.001
中图分类号：
R71 [妇产科学];
学科分类号：
100211 ;
摘要：
The field of clinical genetics has advanced at an unprecedented pace. Today, with the aid of several high-resolution and high-precision technologies, physicians are able to make molecular genetic diagnoses for many infants affected with genetic disease. It is imperative, however, that perinatologists and neonatologists understand the strengths and limitations of genetic testing. This article discusses the different genetic testing options available for perinatal and neonatal diagnostics, along with their clinical utilities and indications. From variant-specific testing to whole-exome and genome sequencing, the article covers the whole gamut of genetic testing, with some thoughts on the changing paradigm of medical genetics.
引用
收藏
页码：217 / +
页数：11
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