Literature DB >> 24300291

Mowat-Wilson syndrome associated with craniosynostosis.

Verity L Hartill1, Maria Pendlebury, Emma Hobson.   

Abstract

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Year:  2014        PMID： 24300291     DOI： 10.1097/MCD.0000000000000016

Source DB:  PubMed          Journal:  Clin Dysmorphol        ISSN： 0962-8827            Impact factor:   0.816


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  4 in total

1.  Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses.

Authors:  Yann Heuzé; Gregory Holmes; Inga Peter; Joan T Richtsmeier; Ethylin Wang Jabs
Journal:  Curr Genet Med Rep       Date:  2014-09-01

Review 2.  Syndromic Craniosynostosis Can Define New Candidate Genes for Suture Development or Result from the Non-specifc Effects of Pleiotropic Genes: Rasopathies and Chromatinopathies as Examples.

Authors:  Marcella Zollino; Serena Lattante; Daniela Orteschi; Silvia Frangella; Paolo N Doronzio; Ilaria Contaldo; Eugenio Mercuri; Giuseppe Marangi
Journal:  Front Neurosci       Date:  2017-10-18       Impact factor: 4.677

Review 3.  Neurological Phenotype of Mowat-Wilson Syndrome.

Authors:  Duccio Maria Cordelli; Veronica Di Pisa; Anna Fetta; Livia Garavelli; Lucia Maltoni; Luca Soliani; Emilia Ricci
Journal:  Genes (Basel)       Date:  2021-06-27       Impact factor: 4.096

4.  A de novo triplication on 2q22.3 including the entire ZEB2 gene associated with global developmental delay, multiple congenital anomalies and behavioral abnormalities.

Authors:  Haiming Yuan; Lina Zhang; Mengfan Chen; Junping Zhu; Zhe Meng; Liyang Liang
Journal:  Mol Cytogenet       Date:  2015-12-23       Impact factor: 2.009
  4 in total

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