Last Posted: Feb 20, 2019
- Application of quality indicators to data from the National Network of Congenital Anomalies of Argentina.
Groisman Boris et al. Birth defects research 2019 Feb - Marfan Syndrome and Loeys-Dietz Syndrome in Children: A Multidisciplinary Team Experience.
Manchola-Linero Alejandra et al. Revista espanola de cardiologia (English ed.) 2018 Jul 71(7) 585-587 - Utilizing Next-Generation Sequencing for the Diagnosis and Clinical Management of Vascular Ehlers-Danlos Syndrome.
Fujita Daishi et al. International heart journal 59(5) 911-913 - Actions in Support of Newborn Screening for Critical Congenital Heart Disease - United States, 2011-2018.
Glidewell Jill et al. MMWR. Morbidity and mortality weekly report 2019 Feb 68(5) 107-111 - Application of next-generation sequencing for the diagnosis of fetuses with congenital heart defects.
Qiao Fengchang et al. Current opinion in obstetrics & gynecology 2019 Jan - Attitudes of clinicians toward cardiac surgery and trisomy 18.
Kaulfus Meagan E et al. Journal of genetic counseling 2019 Jan - The Oculome panel test: next-generation sequencing to diagnose a diverse range of genetic developmental eye disorders.
Patel Aara et al. Ophthalmology 2019 Jan - Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working Group.
Kashtan Clifford E et al. Kidney international 2018 93(5) 1045-1051 - Clinical genetics: DNA sequencing trumps standard screening tools.
Koch Linda et al. Nature reviews. Genetics 2014 May 15(5) 288 - Principles of first trimester screening in the age of non-invasive prenatal diagnosis: screening for chromosomal abnormalities.
Kagan Karl Oliver et al. Archives of gynecology and obstetrics 2017 Oct 296(4) 645-651
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