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Houge-Janssens syndrome.

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Title: Houge-Janssens syndrome.
Authors: Houge GD; Department of Medical Genetics, Haukeland University Hospital, Bergen, Norway. gunnar.houge@helse-bergen.no., Houge SD; Department of Medical Genetics, Haukeland University Hospital, Bergen, Norway., Hsieh TC; Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn, Germany., Verbinnen I; Laboratory of Protein Phosphorylation & Proteomics, Department of Cellular & Molecular Medicine, xc Leuven, Belgium.; KU Leuven Institute for Rare Diseases (Leuven IRD), Leuven, Belgium., Janssens V; Laboratory of Protein Phosphorylation & Proteomics, Department of Cellular & Molecular Medicine, xc Leuven, Belgium. veerle.janssens@kuleuven.be.; KU Leuven Institute for Rare Diseases (Leuven IRD), Leuven, Belgium. veerle.janssens@kuleuven.be.
Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2025 Oct; Vol. 33 (10), pp. 1228-1239. Date of Electronic Publication: 2025 Jun 24.
Publication Type: Journal Article; Review
Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Houge-Janssens syndrome.
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  Data: <searchLink fieldCode="AU" term="%22Houge+GD%22">Houge GD</searchLink>; Department of Medical Genetics, Haukeland University Hospital, Bergen, Norway. gunnar.houge@helse-bergen.no.<br /><searchLink fieldCode="AU" term="%22Houge+SD%22">Houge SD</searchLink>; Department of Medical Genetics, Haukeland University Hospital, Bergen, Norway.<br /><searchLink fieldCode="AU" term="%22Hsieh+TC%22">Hsieh TC</searchLink>; Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn, Germany.<br /><searchLink fieldCode="AU" term="%22Verbinnen+I%22">Verbinnen I</searchLink>; Laboratory of Protein Phosphorylation & Proteomics, Department of Cellular & Molecular Medicine, xc Leuven, Belgium.; KU Leuven Institute for Rare Diseases (Leuven IRD), Leuven, Belgium.<br /><searchLink fieldCode="AU" term="%22Janssens+V%22">Janssens V</searchLink>; Laboratory of Protein Phosphorylation & Proteomics, Department of Cellular & Molecular Medicine, xc Leuven, Belgium. veerle.janssens@kuleuven.be.; KU Leuven Institute for Rare Diseases (Leuven IRD), Leuven, Belgium. veerle.janssens@kuleuven.be.
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  Data: <searchLink fieldCode="JN" term="%229302235%22">European journal of human genetics : EJHG</searchLink> [Eur J Hum Genet] 2025 Oct; Vol. 33 (10), pp. 1228-1239. <i>Date of Electronic Publication: </i>2025 Jun 24.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Nature+Publishing+Group%22">Nature Publishing Group </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9302235 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1476-5438 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210184813%22">10184813 </searchLink><i>NLM ISO Abbreviation: </i>Eur J Hum Genet <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=40555839
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        Value: 10.1038/s41431-025-01901-1
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      – Code: eng
        Text: English
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              Text: 2025 Oct
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