Last Posted: Apr 25, 2019
- Carrier screening for spinal muscular atrophy with a simple test based on melting analysis.
Xia Zhongmin et al. Journal of human genetics 2019 May 64(5) 387-396 - Aberrant DNA methylation as a diagnostic biomarker of diabetic embryopathy.
Schulze Katharina V, et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 4 0. - Community Perspectives on Contraception in the Context of the Zika Virus in the U.S. Virgin Islands: Implications for Communication and Messaging.
Brittain Anna W et al. Women's health issues : official publication of the Jacobs Institute of Women's Health 2019 Mar - Machine Learning Models for Genetic Risk Assessment of Infants with Non-syndromic Orofacial Cleft.
Zhang Shi-Jian et al. Genomics, proteomics & bioinformatics 2018 16(5) 354-364 - Phelan-McDermid syndrome and cancer predisposition: The value of a karyotype.
McKelvey Kent D et al. American journal of medical genetics. Part A 2018 176(1) 144-145 - Predicting deterioration of ventricular function in patients with repaired tetralogy of Fallot using machine learning.
Samad Manar D et al. European heart journal cardiovascular Imaging 2018 19(7) 730-738 - The phenotypic spectrum of proximal 6q deletions based on a large cohort derived from social media and literature reports.
Engwerda Aafke et al. European journal of human genetics : EJHG 2018 26(10) 1478-1489 - Noninvasive Prenatal Testing for Trisomies 21, 18, and 13, Sex Chromosome Aneuploidies, and Microdeletions: A Health Technology Assessment.
et al. Ontario health technology assessment series 2019 19(4) 1-166 - Genetic analysis of Charcot-Marie-Tooth disease in Denmark and the implementation of a next generation sequencing platform.
Vaeth Signe et al. European journal of medical genetics 2019 Jan 62(1) 1-8 - Cell-free fetal DNA versus maternal serum screening for trisomy 21 in pregnant women with and without assisted reproduction technology: a prospective interventional study.
Costa Jean-Marc et al. Genetics in medicine : official journal of the American College of Medical Genetics 2018 20(11) 1346-1353
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