Correction: KAT6A Syndrome: genotype-phenotype correlation in 76 patients with pathogenic KAT6A variants.

Journal

Genetics in medicine : official journal of the American College of Medical Genetics
ISSN: 1530-0366
Titre abrégé: Genet Med
Pays: United States
ID NLM: 9815831

Informations de publication

Date de publication:
Nov 2020
Historique:
pubmed: 21 8 2020
medline: 21 8 2020
entrez: 21 8 2020
Statut: ppublish

Résumé

An amendment to this paper has been published and can be accessed via a link at the top of the paper.

Identifiants

DOI: 10.1038/s41436-020-00944-7 PMID: 32814847
pubmed: 32814847
doi: 10.1038/s41436-020-00944-7
pii: S1098-3600(21)00793-0
doi:

Types de publication

Published Erratum

Langues

eng

Sous-ensembles de citation

IM

Pagination

1920

Commentaires et corrections

Type : ErratumFor

Auteurs

Joanna Kennedy (J)

Clinical Genetics, University Hospitals Bristol, Southwell St, Bristol, UK.
University of Bristol, Bristol, UK.

David Goudie (D)

Clinical Genetics, Ninewells Hospital & Medical School, Dundee, UK.

Edward Blair (E)

Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Department of Clinical Genetics, Churchill Hospital, Headington, Oxford, UK.

Kate Chandler (K)

Manchester Centre for Genomic Medicine, St. Mary's Hospital, Central Manchester Foundation NHS Trust, Manchester Academic Health Science Centre (MAHSC), Manchester, UK.

Shelagh Joss (S)

West of Scotland Genetics Service, Queen Elizabeth University Hospital, Glasgow, UK.

Victoria McKay (V)

Cheshire & Merseyside Regional Genetics Service, Liverpool Women's NHS Foundation Trust, Crown Street, Liverpool, UK.

Andrew Green (A)

Department of Clinical Genetics, Our Lady's Children's Hospital, Crumlin, Dublin, Ireland.
School of Medicine and Medical Science, University College Dublin, Dublin, Ireland.

Ruth Armstrong (R)

East Anglian Medical Genetics Service, Addenbrooke's Hospital, Cambridge, UK.

Melissa Lees (M)

Clinical Genetics, Great Ormond Street Hospital NHS Trust, London, UK.

Benjamin Kamien (B)

Hunter Genetics, Newcastle, Australia.

Bruce Hopper (B)

Hunter Genetics, Newcastle, Australia.

Tiong Yang Tan (TY)

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

Patrick Yap (P)

Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, Australia.
Genetic Health Service New Zealand, Auckland, New Zealand.

Zornitza Stark (Z)

Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, Australia.

Nobuhiko Okamoto (N)

Department of Medical Genetics, Osaka Medical Center, Osaka, Japan.
Research Institute for Maternal and Child Health, Osaka Medical Center, Osaka, Japan.

Noriko Miyake (N)

Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.

Naomichi Matsumoto (N)

Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.

Ellen Macnamara (E)

National Human Genome Research Institute, NIH, Bethesda, MD, USA.

Jennifer L Murphy (JL)

National Human Genome Research Institute, NIH, Bethesda, MD, USA.

Elizabeth McCormick (E)

Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Hakon Hakonarson (H)

Center for Applied Genomics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Marni J Falk (MJ)

Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Dong Li (D)

Center for Applied Genomics, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Patrick Blackburn (P)

Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA.

Eric Klee (E)

Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA.
Department of Clinical Genomics, Mayo Clinic, Rochester, MN, USA.

Dusica Babovic-Vuksanovic (D)

Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA.
Department of Clinical Genomics, Mayo Clinic, Rochester, MN, USA.

Susan Schelley (S)

Division of Medical Genetics, Department of Pediatrics, Stanford University, Stanford, CA, USA.

Louanne Hudgins (L)

Division of Medical Genetics, Department of Pediatrics, Stanford University, Stanford, CA, USA.

Sarina Kant (S)

Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.

Bertrand Isidor (B)

Service de Génétique Médicale, CHU Nantes, Nantes, France.

Benjamin Cogne (B)

Service de Génétique Médicale, CHU Nantes, Nantes, France.

Kimberley Bradbury (K)

Clinical Genetics Guys and St Thomas' NHS Foundation Trust, Guys Hospital, London, UK.

Mark Williams (M)

Molecular Diagnostics, Mater Group, South Brisbane, Queensland, Australia.

Chirag Patel (C)

Genetic Health Queensland, Herston, Brisbane, Queensland, Australia.

Helen Heussler (H)

Child Development Service, Lady Cilento Children's Hospital, Brisbane, Queensland, Australia.

Celia Duff-Farrier (C)

Bristol Genetics Laboratory, Southmead Hospital, Bristol, UK.

Phillis Lakeman (P)

Academic Medical Center, Department of Clinical Genetics, Amsterdam, The Netherlands.

Ingrid Scurr (I)

Clinical Genetics, University Hospitals Bristol, Southwell St, Bristol, UK.

Usha Kini (U)

Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Department of Clinical Genetics, Churchill Hospital, Headington, Oxford, UK.

Mariet Elting (M)

Klinisch Geneticus, VU Medisch centrum, Amsterdam, The Netherlands.

Margot Reijnders (M)

Radboud University Medical Center, Department of Human Genetics, Nijmegen, The Netherlands.

Janneke Schuurs-Hoeijmakers (J)

Radboud University Medical Center, Department of Human Genetics, Nijmegen, The Netherlands.

Mohamed Wafik (M)

Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Department of Clinical Genetics, Churchill Hospital, Headington, Oxford, UK.

Anne Blomhoff (A)

Department of Medical Genetics, Oslo University Hospital, Oslo, Norway.

Claudia A L Ruivenkamp (CAL)

Klinische Genetica, Leiden University, Leiden, The Netherlands.

Esther Nibbeling (E)

Department of Genetics, University of Groningen, Groningen, The Netherlands.

Alexander J M Dingemans (AJM)

Radboud University Medical Center, Department of Human Genetics, Nijmegen, The Netherlands.

Emilie D Douine (ED)

Department of Human Genetics, David Geffen School of Medicine, UCLA, Los Angeles, CA, USA.

Stanley F Nelson (SF)

Department of Human Genetics, David Geffen School of Medicine, UCLA, Los Angeles, CA, USA.
Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, UCLA, Los Angeles, CA, USA.

Maja Hempel (M)

Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, 20246, Hamburg, Germany.

Tatjana Bierhals (T)

Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, 20246, Hamburg, Germany.

Davor Lessel (D)

Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, 20246, Hamburg, Germany.

Jessika Johannsen (J)

Department of Pediatrics, University Medical Center Hamburg-Eppendorf, 20246, Hamburg, Germany.

Valerie A Arboleda (VA)

Department of Human Genetics, David Geffen School of Medicine, UCLA, Los Angeles, CA, USA. varboleda@mednet.ucla.edu.
Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, UCLA, Los Angeles, CA, USA. varboleda@mednet.ucla.edu.

Ruth Newbury-Ecob (R)

Clinical Genetics, University Hospitals Bristol, Southwell St, Bristol, UK. Ruth.Newbury-Ecob@UHBristol.nhs.uk.
University of Bristol, Bristol, UK. Ruth.Newbury-Ecob@UHBristol.nhs.uk.

Classifications MeSH