Rapid Identification of Biallelic

Hereditary spherocytosis Medical genomics Rapid exome sequencing Red cell membrane defects Red cells

Journal

Molecular syndromology
ISSN: 1661-8769
Titre abrégé: Mol Syndromol
Pays: Switzerland
ID NLM: 101525192

Informations de publication

Date de publication:
Feb 2020
Historique:
accepted: 05 12 2019
entrez: 8 4 2020
pubmed: 8 4 2020
medline: 8 4 2020
Statut: ppublish

Résumé

Heterozygous pathogenic variants in

Identifiants

pubmed: 32256302
doi: 10.1159/000505886
pii: msy-0011-0050
pmc: PMC7109415
doi:

Types de publication

Journal Article

Langues

eng

Pagination

50-55

Informations de copyright

Copyright © 2020 by S. Karger AG, Basel.

Déclaration de conflit d'intérêts

The authors have no conflicts of interest to declare.

Références

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Auteurs

Christopher M Richmond (CM)

Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, Australia.
School of Medicine, Griffith University, Gold Coast, Australia.

Sally Campbell (S)

Department of Haematology, Royal Children's Hospital, Melbourne, Australia.

Hee W Foo (HW)

Department of Gastroenterology, Royal Children's Hospital, Melbourne, Australia.

Sebastian Lunke (S)

Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, Australia.
Department of Clinical Pathology, University of Melbourne, Melbourne, Australia.
Australian Genomics Health Alliance, Parkville, Australia.

Zornitza Stark (Z)

Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, Australia.
Australian Genomics Health Alliance, Parkville, Australia.
Department of Paediatrics, University of Melbourne, Melbourne, Australia.

Amanda Moody (A)

Department of Neonatal Medicine, Royal Children's Hospital, Melbourne, Australia.

Elizabeth Bannister (E)

Department of Gastroenterology, Royal Children's Hospital, Melbourne, Australia.
Department of Paediatrics, University of Melbourne, Melbourne, Australia.

Anthea Greenway (A)

Department of Haematology, Royal Children's Hospital, Melbourne, Australia.

Natasha Brown (N)

Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, Australia.
Department of Paediatrics, University of Melbourne, Melbourne, Australia.

Classifications MeSH