Publisher Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

QR Code

Publisher Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease

Saved in:

Bibliographic Details
Main Authors:	Nathaly M. Sweeney, Shareef A. Nahas, Shimul Chowdhury, Sergey Batalov, Michelle Clark, Sara Caylor, Julie Cakici, John J. Nigro, Yan Ding, Narayanan Veeraraghavan, Charlotte Hobbs, David Dimmock, Stephen F. Kingsmore
Format:	article
Language:	EN
Published:	Nature Portfolio 2021
Subjects:	Medicine R Genetics QH426-470
Online Access:	https://doaj.org/article/5c84196fbd2942d9ad984aa6da8cb7f5
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items

Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease
by: Nathaly M. Sweeney, et al.
Published: (2021)

Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease
by: Nathaly M. Sweeney, et al.
Published: (2021)

Case Report: An Infant With Kabuki Syndrome, Alobar Holoprosencephaly and Truncus Arteriosus: A Case for Whole Exome Sequencing in Neonates With Congenital Anomalies
by: Rishika P. Sakaria, et al.
Published: (2021)

Blood genome expression profiles in infants with congenital cytomegalovirus infection
by: Christopher P. Ouellette, et al.
Published: (2020)

Infants with congenital heart defects have reduced brain volumes
by: Mikkel B. Skotting, et al.
Published: (2021)

Persistent pleural effusion in an infant with an unusual diagnosis: congenital alveolar rhabdomyosarcoma
by: Can Yozgat, et al.
Published: (2020)

Extensive genome-wide variability of human cytomegalovirus in congenitally infected infants.
by: Nicholas Renzette, et al.
Published: (2011)

Different characteristics of infants diagnosed with congenital choledochal malformation prenatally or postnatally
by: Wei Chen, et al.
Published: (2021)

Ultrasound biomicroscopy as a diagnostic tool in infants with primary congenital glaucoma
by: Hussein TR, et al.
Published: (2014)

Surgical management of a massive congenital hemangioma of the tongue in an infant: A rare case report
by: Krishan Sarna, et al.
Published: (2021)

Cerebral oxygen saturation and cerebrovascular instability in newborn infants with congenital heart disease compared to healthy controls.
by: Nhu N Tran, et al.
Published: (2021)

A case report describing the immune response of an infant with congenital heart disease and severe COVID-19
by: Danielle Wurzel, et al.
Published: (2021)

Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome
by: Cristina E. Trevino, et al.
Published: (2021)

The size-weight illusion is unimpaired in individuals with a history of congenital visual deprivation
by: Rashi Pant, et al.
Published: (2021)

Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism.
by: Maria Carla Proverbio, et al.
Published: (2013)

The Association of Positive or Negative Religious Coping Methods With Psychological Distress and Quality of Life Among Parents of Infants With Congenital Heart Disease
by: Jian-Feng Liu, et al.
Published: (2021)

The rate of symptomatic improvement of congenital nasolacrimal duct obstruction in Japanese infants treated with conservative management during the 1st year of age
by: Hirohiko Kakizaki, et al.
Published: (2008)

Whole blood gene expression profiles to assess pathogenesis and disease severity in infants with respiratory syncytial virus infection.
by: Asuncion Mejias, et al.
Published: (2013)

Identification of candidate genes and pathways in retinopathy of prematurity by whole exome sequencing of preterm infants enriched in phenotypic extremes
by: Sang Jin Kim, et al.
Published: (2021)

Delayed presentation of congenital rectal stenosis associated with Down's syndrome and hypothyroidism: Case report
by: Tanvir Kabir Chowdhury, et al.
Published: (2021)

Biallelic mutations in valyl-tRNA synthetase gene VARS are associated with a progressive neurodevelopmental epileptic encephalopathy
by: Jennifer Friedman, et al.
Published: (2019)

Evidence base for specific pulmonary vasodilators in adults with congenital heart disease
by: Anton A. Shmalts, et al.
Published: (2021)

Correction to: Combination of the endoscopic septonasal flap technique and bioabsorbable steroid-eluting stents for repair of congenital choanal atresia in neonates and infants: a retrospective study
by: Peng-peng Wang, et al.
Published: (2021)

AN OVERVIEW OF METACOGNITIVE STRATEGIES IN READING COMPREHENSION SKILL
by: Dilek ÇAKICI
Published: (2019)

Congenital adrenal hyperplasia
by: Miolski Jelena, et al.
Published: (2021)

Congenital heart disease
Published: (2006)

Incidence of Congenital Malformations
by: Flor de María Cáceres, et al.
Published: (1999)

Congenital intrascleral cyst
by: Akbaba M, et al.
Published: (2011)

Publisher Correction: Five-month-old infants detect affiliation in colaughter
by: Athena Vouloumanos, et al.
Published: (2019)

Long-term outcome of primary intraocular lens implantation in bilateral congenital cataract in infants with a median age of 35 days at surgery: a case series
by: Liv Drolsum, et al.
Published: (2021)

Publisher Correction: Analysis of the shape of the T-wave in congenital long-QT syndrome type 3 by geometric morphometrics
by: Hitoshi Horigome, et al.
Published: (2021)

Multiple Congenital Heart Abnormalities
by: Lazarov S., et al.
Published: (2019)

Congenital nystagmus and negative electroretinography
by: Roussi M, et al.
Published: (2011)

THE EVALUATION OF CONGENITAL NEUTROPENIA PATIENTS
by: Nihal Karadaş, et al.
Published: (2021)

Infant observation

Atrial Fibrillation in Congenital Heart Disease
by: Irene Martín de Miguel, et al.
Published: (2021)

Critical congenital heart disease screening
by: Mohammed A Chamsi-Pasha, et al.
Published: (2016)

An Atypical Case of Congenital Erythropoietic Porphyria
by: Bénédicte Sudrié-Arnaud, et al.
Published: (2021)

Dermoscopy of Congenital Langerhans Cell Histiocytosis
by: Ramon Pigem, et al.
Published: (2020)

Spitz and Reed nevi: acquired or congenital?
by: Michael Bär
Published: (2012)