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Genomic Testing in Children
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Last Updated: Jan 07, 2016
- Whole-Genome Sequencing and Disability in the NICU: Exploring Practical and Ethical Challenges
MJ Deem. Pediatrics, January 2016 (From Discoveries and Insights Database)
- Parental Views on Expanded Newborn Screening Using Whole-Genome Sequencing
G Joseph et al. Pediatrics, January 2016 (From Discoveries and Insights Database)
- Potential Psychosocial Risks of Sequencing Newborns
SA Wasibren et al. Pediatrics, January 2016 (From Discoveries and Insights Database)
- Supporting Parental Decisions About Genomic Sequencing for Newborn Screening: The NC NEXUS Decision Aid
MA Lewis et al, Pediatrics, January 2016 (From Discoveries and Insights Database)
- Whole-Genome Screening of Newborns? The Constitutional Boundaries of State Newborn Screening Programs
JS King et al. Pediatrics, January 2016 (From Discoveries and Insights Database)
- The Challenge of Analyzing the Results of Next-Generation Sequencing in Children
I Thiffaut et al. Pediatrics, January 2016 (From Discoveries and Insights Database)
- Introduction to Bioethics Special Supplement V: Ethical Issues in Genomic Testing of Children
JD Lantos, Pediatrics, January 2016 (From Discoveries and Insights Database)
- The psychological impact of genetic information on children: a systematic review
CE Wakefield et al, Genetics in Medicine, January 7, 2016 (From Discoveries and Insights Database)
- Introduction to Bioethics Special Supplement V: Ethical Issues in Genomic Testing of Children.
Lantos John D et al. Pediatrics 2016 Jan 137 Suppl 1S1-2 (From Genomics & Health Impact Scan Database)
- Ashkenazi Jewish population screening for Tay-Sachs disease: the international and Australian experience.
Lew Raelia M et al. Journal of paediatrics and child health 2015 Mar 51(3) 271-9 (From Genomics & Health Impact Scan Database)
- Genetic Polymorphisms of Toll-like Receptor 4 are Associated with Respiratory Syncytial Virus Infection in a Chinese Infant Population.
Zhu Hua, et al. Clinical laboratory 2015 0 (10) 1391-9 (From HuGE Literature Finder)
- A diagnostic approach for cerebral palsy in the genomic era.
Lee Ryan W et al. Neuromolecular medicine 2014 Dec (4) 821-44 (From Discoveries and Insights Database)
- Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network.
Gallego Carlos J et al. American journal of human genetics 2015 Oct (4) 512-20 (From Discoveries and Insights Database)
- [Genetically determined lipid metabolism disorders due to oral intake of technogenic hyperchlorination products].
Luzhetsky K P, et al. Meditsina truda i promyshlennaia ekologiia 2015 0 (8) 24-8 (From HuGE Literature Finder)
- [Clinical and laboratory diagnostic criteria of chronic glomerular and tubulointerstitial kidney disorders associated with exposure to metals and oxygen organic compounds of technogenic origin].
Ustinova O Yu, et al. Meditsina truda i promyshlennaia ekologiia 2015 0 (8) 33-8 (From HuGE Literature Finder)
- [SMN1 Gene Point Mutations in Type I-IV Proximal Spinal Muscular Atrophy Patients with a Single Copy of SMN1].
Genetika 2015 9 (9) 1075-82 (From HuGE Literature Finder)
- Conversations with children about DNA and genes using an original children's book.
Newcomb Patricia et al. Journal of pediatric health care : official publication of National Association of Pediatric Nurse Associates & Practitioners 28(6) 497-506 (From Genomics & Health Impact Scan Database)
- The validity of family history as a risk factor in pediatric hearing loss.
Driscoll Carlie et al. International journal of pediatric otorhinolaryngology 2015 May 79(5) 654-9 (From Genomics & Health Impact Scan Database)
- Developments in understanding acquired immunity and innate susceptibility to norovirus and rotavirus gastroenteritis in children.
Payne Daniel C et al. Current opinion in pediatrics 2015 Feb (1) 105-9 (From Discoveries and Insights Database)
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