Last Posted: Aug 02, 2018
- First trimester combined screening for fetal aneuploidies enhanced with additional ultrasound markers: an 8-year prospective study.
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Wang Yan et al. American journal of obstetrics and gynecology 2018 218(2) 244.e1-244.e17 - The Combining Effects of Cell-Free Circulating Tumor DNA of Breast Tumor to the Noninvasive Prenatal Testing Results: A Simulating Investigation.
Cai Ya-Hong et al. DNA and cell biology 2018 Jul 37(7) 626-633 - A Framework for Describing the Influence of Service Organisation and Delivery on Participation in Fetal Anomaly Screening in England.
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Xu B et al. Lin chuang er bi yan hou tou jing wai ke za zhi = Journal of clinical otorhinolaryngology, head, and neck surgery 2018 Jun 32(11) 811-815 - Combined genetic analyses can achieve efficient diagnostic yields for subjects with Alagille syndrome and incomplete Alagille syndrome.
Ohashi Kei et al. Acta paediatrica (Oslo, Norway : 1992) 2017 Nov 106(11) 1817-1824 - Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencing.
Haggerty Christopher M et al. Genetics in medicine : official journal of the American College of Medical Genetics 2017 Nov 19(11) 1245-1252 - Evaluation of C26:0-lysophosphatidylcholine and C26:0-carnitine as diagnostic markers for Zellweger spectrum disorders.
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