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Genes|April 12, 2020
The Impact of the CFTR Gene Discovery on Cystic Fibrosis Diagnosis, Counseling, and Preventive TherapyPhilip M Farrell, Michael J Rock, Mei W BakerInternational Journal of Neonatal Screening|October 30, 2020
Translating Molecular Technologies into Routine Newborn Screening PracticeSarah M Furnier, Maureen S Durkin, Mei W BakerInternational Journal of Neonatal Screening|July 21, 2021
Newborn Screening for Severe Combined Immunodeficiency: Do Preterm Infants Require Special Consideration?Anne E Atkins, Michael F Cogley, Mei W BakerInternational Journal of Neonatal Screening|October 26, 2021
Correction: Furnier et al. Translating Molecular Technologies into Routine Newborn Screening Practice. Int. J. Neonatal Screen. 2020, 6, 80Sarah M Furnier, Maureen S Durkin, Mei W BakerClinica Chimica Acta; International Journal of Clinical Chemistry|June 3, 2014
Development of an assay to simultaneously measure orotic acid, amino acids, and acylcarnitines in dried blood spotsPatrice K Held, Christopher A Haynes, Víctor R De Jesús, et al.Journal of Clinical Immunology|September 30, 2011
Cause of death in neonates with inconclusive or abnormal T-cell receptor excision circle assays on newborn screeningDeborah J Accetta, Charles D Brokopp, Mei W Baker, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 11, 2011
Optimal DNA tier for the IRT/DNA algorithm determined by CFTR mutation results over 14 years of newborn screeningMei W Baker, Molly Groose, Gary Hoffman, et al.International Journal of Neonatal Screening|April 25, 2022
Newborn Screen for X-Linked Adrenoleukodystrophy Using Flow Injection Tandem Mass Spectrometry in Negative Ion ModeTarek A Teber, Brian J Conti, Christopher A Haynes, et al.American Journal of Medical Genetics. Part A|April 25, 2013
Novel mutation in TP63 associated with ectrodactyly ectodermal dysplasia and clefting syndrome and T cell lymphopeniaPhilip F Giampietro, Mei W Baker, Monica J Basehore, et al.The Journal of Pediatrics|December 24, 2018
Increased Congenital Hypothyroidism Detection in Preterm Infants with Serial Newborn ScreeningDinushan C Kaluarachchi, David B Allen, Jens C Eickhoff, et al.Pageof 3