Last Posted: Sep 06, 2018
- What do women (and men) want? Parents weigh in on genetic testing for rare diseases in children
S Grosse, CDC Blog, 2018 - Eugenics Redux: "Reproductive Benefit" as a Rationale for Newborn Screening.
Paul Diane B et al. The Hastings Center report 2018 Jul 48 Suppl 2S12-S13 - Families' Experiences with Newborn Screening: A Critical Source of Evidence.
Grob Rachel et al. The Hastings Center report 2018 Jul 48 Suppl 2S29-S31 - Lessons for Sequencing from the Addition of Severe Combined Immunodeficiency to Newborn Screening Panels.
Puck Jennifer M et al. The Hastings Center report 2018 Jul 48 Suppl 2S7-S9 - Newborn blood spot screening for cystic fibrosis with a four-step screening strategy in the Netherlands.
Dankert-Roelse Jeannette E et al. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2018 Aug - Newborn screening by tandem mass spectrometry confirms the high prevalence of sickle cell disease among German newborns.
Lobitz Stephan et al. Annals of hematology 2018 Aug - Newborn screening for Cerebrotendinous Xanthomatosis is the Solution for Early Identification and Treatment.
DeBarber Andrea E et al. Journal of lipid research 2018 Aug - Sequencing Newborns: A Call for Nuanced Use of Genomic Technologies.
Johnston Josephine et al. The Hastings Center report 2018 Jul 48 Suppl 2S2-S6 - Single-Gene Sequencing in Newborn Screening: Success, Challenge, Hope.
Currier Robert J et al. The Hastings Center report 2018 Jul 48 Suppl 2S37-S38 - The Legal Dimensions of Genomic Sequencing in Newborn Screening.
Zacharias Rachel L et al. The Hastings Center report 2018 Jul 48 Suppl 2S39-S41
No hay comentarios:
Publicar un comentario