Literature DB >> 14684701

Rapp-Hodgkin and AEC syndromes due to a new frameshift mutation in the TP63 gene.

I Dianzani1, E Garelli, P Gustavsson, A Carando, B Gustafsson, N Dahl, G Annerén.   

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Year:  2003        PMID： 14684701      PMCID： PMC1735338          DOI： 10.1136/jmg.40.12.e133

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  4 in total

Review 1.  Integrating animal models and in vitro tissue models to elucidate the role of desmosomal proteins in diseases.

Authors:  Maranke I Koster; Jason Dinella; Jiangli Chen; Charlene O'Shea; Peter J Koch
Journal:  Cell Commun Adhes       Date:  2014-02

Review 2.  Modeling AEC-New approaches to study rare genetic disorders.

Authors:  Peter J Koch; Jason Dinella; Mary Fete; Elaine C Siegfried; Maranke I Koster
Journal:  Am J Med Genet A       Date:  2014-03-24       Impact factor: 2.802

3.  Ectodermal Dysplasia Showing the Clinical Overlap between Hay Wells Syndrome and Bowen Armstrong Syndrome.

Authors:  Andreea Liana Rachisan; Simona Cainap; Mariana Andreica; Nicolae Miu
Journal:  Iran J Pediatr       Date:  2011-03       Impact factor: 0.364

4.  Differentially Expressed Genes in EEC and LMS Syndromes.

Authors:  Wei Yin; Yaling Song; Yangge Du; Zhuan Bian
Journal:  PLoS One       Date:  2015-06-15       Impact factor: 3.240
  4 in total

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