Associated Papers
Exome sequencing improves genetic diagnosis of fetal increased nuchal translucency.
Yang X et al.
Prenatal Diagnosis, 2020
[Rapid genetic prenatal diagnosis for achondroplasia].
Zhu HY et al.
Zhonghua Fu Chan Ke Za Zhi, 2008
Association of single nucleotide polymorphisms in endothelin family genes with the progression of atherosclerosis in patients with essential hypertension.
Yasuda H et al.
Journal of Human Hypertension, 2007
Association of genetic polymorphisms of endothelin-converting enzyme-1 gene with hypertension in a Japanese population and rare missense mutation in preproendothelin-1 in Japanese hypertensives.
Banno M et al.
Hypertension Research : Official Journal of the Japanese Society of Hypertension, 2007
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