A previously undescribed de novo 4p15 deletion in a patient with apparently isolated metopic craniosynostosis

Author:

Alesi Viola,Barrano Giuseppe,Morara Sara,Darelli Daria,Petrilli Katia,Capalbo Anna,Pacella Mario,Haass Cristina,Finocchi Maurizio,Novelli Antonio,Bertoli Marta

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference50 articles.

1. Case report: Cytogenetic and molecular analysis of proximal interstitial deletion of 4p, review of the literature and comparison with Wolf-Hirschhorn syndrome;Bailey;J Assoc Genet Technol,2010

2. Syndromic craniosynostosis due to complex chromosome 5 rearrangement and MSX2 gene triplication;Bernardini;Am J Med Genet Part A,2007

3. Array-based comparative genomic hybridization in early-stage mycosis fungoides: Recurrent deletion of tumor suppressor genes BCL7A, SMAC/DIABLO, and RHOF;Carbone;Genes Chromosomes Cancer,2008

4. Syndrome of proximal interstitial deletion 4p15: Report of three cases and review of the literature;Chitayat;Am J Med Genet,1995

5. Genetics of craniosynostosis: Review of the literature;Ciurea;J Med Life,2009

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