Literature DB >> 19006215

Recurrence of Mowat-Wilson syndrome in siblings with a novel mutation in the ZEB2 gene.

Massimiliano Cecconi1, Francesca Forzano, Livia Garavelli, Chiara Pantaleoni, Marina Grasso, Franca Dagna Bricarelli, Lucia Perroni, Emilio Di Maria, Francesca Faravelli.   

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Year:  2008        PMID： 19006215     DOI： 10.1002/ajmg.a.32568

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  5 in total

Review 1.  Hirschsprung's disease in children with Mowat-Wilson syndrome.

Authors:  David Coyle; Prem Puri
Journal:  Pediatr Surg Int       Date:  2015-07-09       Impact factor: 1.827

2.  IL-12 selectively programs effector pathways that are stably expressed in human CD8+ effector memory T cells in vivo.

Authors:  Fatema Z Chowdhury; Hilario J Ramos; Laurie S Davis; James Forman; J David Farrar
Journal:  Blood       Date:  2011-08-10       Impact factor: 22.113

Review 3.  Chromosomal and related Mendelian syndromes associated with Hirschsprung's disease.

Authors:  S W Moore
Journal:  Pediatr Surg Int       Date:  2012-09-23       Impact factor: 1.827

4.  Experience of Mowat-Wilson syndrome prenatal diagnosis for a Chinese family.

Authors:  Qian Jiang; Xiaoxiao Zhang; Yinan Ma; Qi Li; Chunhua Zheng; Yuchun Yan; Zhen Zhang; Ping Xiao; Lin Su; Wei Cheng; Hong Pan; Long Li
Journal:  Clin Case Rep       Date:  2016-11-17

5.  Anaesthetic management of Mowat-Wilson syndrome.

Authors:  Amit Sudhir Deshmukh; Kalpna Vinod Kelkar; Sunita M Khedkar; Yogesh Gavali
Journal:  Indian J Anaesth       Date:  2016-04
  5 in total

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