Last Posted: Jul 20, 2017
- Baby Genome Sequencing for Sale in China
A Regalado, MIT Review, June, 2017 - Idiopathic T cell lymphopenia identified in New York State Newborn Screening.
Albin-Leeds Stephanie et al. Clinical immunology (Orlando, Fla.) 2017 Jul - Presymptomatic Diagnosis of Spinal Muscular Atrophy Through Newborn Screening.
Chien Yin-Hsiu et al. The Journal of pediatrics 2017 Jul - Baby genome screening - paving the way to genetic discrimination?
MG Seidel, BMJ Opinion July 5, 2017 - Expanded Newborn Screening: Information and Resources for the Family Physician.
Weismiller David Glenn et al. American family physician 2017 Jun 95(11) 703-709 - Laboratory diagnosis of biotinidase deficiency, 2017 update: a technical standard and guideline of the American College of Medical Genetics and Genomics.
Strovel Erin T et al. Genetics in medicine : official journal of the American College of Medical Genetics 2017 Jul - Neonatal screening improves sickle cell disease clinical outcome in Belgium.
Lê Phu-Quoc et al. Journal of medical screening 2017 Jan 969141317701166 - Baby genome screeningpaving the way to genetic discrimination?
MG Seidel, BMJ Opinion July 5, 2017 - Impairment Experiences, Identity and Attitudes Towards Genetic Screening: the Views of People with Spinal Muscular Atrophy.
Boardman Felicity K et al. Journal of genetic counseling 2017 Jun - Introduction of a Simple Second Tier Screening Test for C5 Isobars in Dried Blood Spots: Reducing the False Positive Rate for Isovaleric Acidaemia in Expanded Newborn Screening.
Carling R S et al. JIMD reports 2017 Jun - Utilization of genomic sequencing for population screening of immunodeficiencies in the newborn.
Pavey Ashleigh R et al. Genetics in medicine : official journal of the American College of Medical Genetics 2017 Jun - Policy brief: Improve coverage of newborn genetic screening to include the Recommended Uniform Screening Panel and newborn screening registry.
Starkweather Angela et al. Nursing outlook 2017 May - Evolving locally appropriate models of care for indian sickle cell disease.
Serjeant Graham R et al. The Indian journal of medical research 2016 Apr 143(4) 405-13 - Identification of 22q11.2 Deletion Syndrome via Newborn Screening for Severe Combined Immunodeficiency.
Barry Jessica C et al. Journal of clinical immunology 2017 May - Sweat test and cystic fibrosis: overview of test performance at public and private centers in the state of São Paulo, Brazil.
Servidoni Maria Fátima et al. Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia 43(2) 121-128 - Paper-Based Diagnostics: Rethinking Conventional Sickle Cell Screening to Improve Access to High-Quality Health Care in Resource-Limited Settings.
Piety Nathaniel Z et al. IEEE pulse 8(3) 42-46
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