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Correction: The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome

Research output: Contribution to journalJournal articleResearchpeer-review

  1. The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Noncardiac genetic predisposition in sudden infant death syndrome

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. The landscape of epilepsy-related GATOR1 variants

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care

    Research output: Contribution to journalJournal articleResearchpeer-review

  1. The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Neonatal hyperinsulinemic hypoglycemia in a patient with 9p deletion syndrome

    Research output: Contribution to journalJournal articleResearchpeer-review

  • Pleuntje J van der Sluijs
  • Sandra Jansen
  • Samantha A Vergano
  • Miho Adachi-Fukuda
  • Yasemin Alanay
  • Adila AlKindy
  • Anwar Baban
  • Allan Bayat
  • Stefanie Beck-Wödl
  • Katherine Berry
  • Emilia K Bijlsma
  • Levinus A Bok
  • Alwin F J Brouwer
  • Ineke van der Burgt
  • Philippe M Campeau
  • Natalie Canham
  • Krystyna Chrzanowska
  • Yoyo W Y Chu
  • Brain H Y Chung
  • Karin Dahan
  • Marjan De Rademaeker
  • Anne Destree
  • Tracy Dudding-Byth
  • Rachel Earl
  • Nursel Elcioglu
  • Ellen R Elias
  • Christina Fagerberg
  • Alice Gardham
  • Blanca Gener
  • Erica H Gerkes
  • Ute Grasshoff
  • Arie van Haeringen
  • Karin R Heitink
  • Johanna C Herkert
  • Nicolette S den Hollander
  • Denise Horn
  • David Hunt
  • Sarina G Kant
  • Mitsuhiro Kato
  • Hülya Kayserili
  • Rogier Kersseboom
  • Esra Kilic
  • Malgorzata Krajewska-Walasek
  • Kylin Lammers
  • Lone W Laulund
  • Damien Lederer
  • Melissa Lees
  • Vanesa López-González
  • Saskia Maas
  • Grazia M S Mancini
  • Carlo Marcelis
  • Francisco Martinez
  • Isabelle Maystadt
  • Marianne McGuire
  • Shane McKee
  • Sarju Mehta
  • Kay Metcalfe
  • Jeff Milunsky
  • Seiji Mizuno
  • John B Moeschler
  • Christian Netzer
  • Charlotte W Ockeloen
  • Barbara Oehl-Jaschkowitz
  • Nobuhiko Okamoto
  • Sharon N M Olminkhof
  • Carmen Orellana
  • Laurent Pasquier
  • Caroline Pottinger
  • Vera Riehmer
  • Stephen P Robertson
  • Maian Roifman
  • Caroline Rooryck
  • Fabienne G Ropers
  • Monica Rosello
  • Claudia A L Ruivenkamp
  • Mahmut S Sagiroglu
  • Suzanne C E H Sallevelt
  • Amparo Sanchis Calvo
  • Pelin O Simsek-Kiper
  • Gabriela Soares
  • Lucia Solaeche
  • Fatma Mujgan Sonmez
  • Miranda Splitt
  • Duco Steenbeek
  • Alexander P A Stegmann
  • Constance T R M Stumpel
  • Saori Tanabe
  • Eyyup Uctepe
  • G Eda Utine
  • Hermine E Veenstra-Knol
  • Sunita Venkateswaran
  • Catheline Vilain
  • Catherine Vincent-Delorme
  • Anneke T Vulto-van Silfhout
  • Patricia Wheeler
  • Golder N Wilson
  • Louise C Wilson
  • Bernd Wollnik
  • Tomoki Kosho
  • Dagmar Wieczorek
  • Evan Eichler
  • Rolph Pfundt
  • Bert B A de Vries
  • Jill Clayton-Smith
  • Gijs W E Santen
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The original version of this Article contained an error in the spelling of the author Pleuntje J. van der Sluijs, which was incorrectly given as Eline (P. J.) van der Sluijs. This has now been corrected in both the PDF and HTML versions of the Article.

Original languageEnglish
JournalGenetics in medicine : official journal of the American College of Medical Genetics
Volume21
Issue number9
Pages (from-to)2160-2161
Number of pages2
ISSN1098-3600
DOIs
Publication statusPublished - Sep 2019

ID: 56412994