Correction: Furnier et al. Translating Molecular Technologies into Routine Newborn Screening Practice. <i>Int. J. Neonatal Screen</i>. 2020, <i>6</i>, 80
In the original article [...]
Saved in:
Main Authors: | Sarah M. Furnier (Author), Maureen S. Durkin (Author), Mei W. Baker (Author) |
---|---|
Format: | Book |
Published: |
MDPI AG,
2021-10-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Translating Molecular Technologies into Routine Newborn Screening Practice
by: Sarah M. Furnier, et al.
Published: (2020) -
Correction: Spenger et al. Glutaric Aciduria Type I Missed by Newborn Screening: Report of Four Cases from Three Families. <i>Int. J. Neonatal Screen</i>. 2021, <i>7</i>, 32
by: Johannes Spenger, et al.
Published: (2021) -
Comment on Jones et al. Application of a Novel Algorithm for Expanding Newborn Screening for Inherited Metabolic Disorders across Europe. <i>Int. J. Neonatal Screen.</i> 2022, <i>8</i>, 20
by: Rose Maase, et al.
Published: (2023) -
Reply to Maase et al. Comment on "Jones et al. Application of a Novel Algorithm for Expanding Newborn Screening for Inherited Metabolic Disorders across Europe. <i>Int. J. Neonatal Screen.</i> 2022, <i>8</i>, 20"
by: Simon A. Jones, et al.
Published: (2023) -
The Role of Extended <i>CFTR</i> Gene Sequencing in Newborn Screening for Cystic Fibrosis
by: Anne Bergougnoux, et al.
Published: (2020)