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De novo and biallelic DEAF1 variants cause a phenotypic spectrum
2019
33 citations
Journal Article
bronze Open Access
Field-Weighted Citation Impact:
2.87
De novo and biallelic DEAF1 variants cause a phenotypic spectrum | Researchclopedia
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University Medical Center Utrecht
Randi J. Hagerman
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University of California Davis Medical Center
Rachel Harrison
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Nottingham University Hospitals NHS Trust
Tara Montgomery
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Newcastle upon Tyne Hospitals NHS Foundation Trust
Miranda Splitt
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Newcastle upon Tyne Hospitals NHS Foundation Trust
Elizabeth E. Palmer
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UNSW Sydney
Rani Sachdev
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UNSW Sydney
Heather C. Mefford
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University of Washington
Abbey Scott
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Seattle Children's Hospital
Julián A. Martínez-Agosto
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University of California, Los Angeles
Rüdiger Lorenz
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Werner-Wicker-Klinik
Naama Orenstein
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Tel Aviv University
Jonathan Berg
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University of Dundee
Jeanne Amiel
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Hôpital Necker-Enfants Malades
Delphine Héron
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Sorbonne Université
Boris Keren
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Sorbonne Université
Jan-Maarten Cobben
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London North West Healthcare NHS Trust
Leonie A. Menke
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Amsterdam University Medical Centers
Elysa J. Marco
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Dominican University of California
John M. Graham
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Cedars-Sinai Medical Center
Tyler Mark Pierson
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Cedars-Sinai Medical Center
Ehsan Ghayoor Karimiani
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St George's, University of London
Reza Maroofian
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St George's, University of London
M. Chiara Manzini
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George Washington University
Edmund Cauley
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George Washington University
Roberto Colombo
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Agostino Gemelli University Polyclinic
Sylvie Odent
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Centre National de la Recherche Scientifique
Christèle Dubourg
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Centre National de la Recherche Scientifique
Chanika Phornphutkul
·
Brown University
Arjan P.M. de Brouwer
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Radboud University Nijmegen
Bert B.A. de Vries
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Radboud University Nijmegen
Anneke T. Vulto-vanSilfhout
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Radboud University Nijmegen