Currarino syndrome: does the presence of a genetic anomaly correlate with a more severe phenotype? A multicentre study-Reference-Cited by-同舟云学术

Currarino syndrome: does the presence of a genetic anomaly correlate with a more severe phenotype? A multicentre study

Published:2017-10 Issue:10 Volume:52 Page:1591-1596
ISSN:0022-3468
Container-title:Journal of Pediatric Surgery
language:en
Short-container-title:Journal of Pediatric Surgery

Author:

Costanzo Sara,Spaccini Luigina,Pio Luca,Mattioli Girolamo,Virgone Calogero,Dall’Igna Patrizia,Iacobelli Barbara,Inserra Alessandro,Brisighelli Giulia,Fagnani Anna Maria,Leva Ernesto,Giannotti Giulia,Cheli Maurizio^ORCID,Frumento Paolo,Riccipetitoni Giovanna

Publisher

Elsevier BV

Subject

General Medicine,Pediatrics, Perinatology and Child Health,Surgery

Reference26 articles.

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2. Currarino syndrome: proposal of a diagnostic and therapeutic protocol;Martucciello;J Pediatr Surg,2004

3. Novel MNX1 mutations and clinical analysis of familial and sporadic Currarino cases;Merello;Eur J Med Genet,2013

4. Sacral agenesis and caudal spinal cord malformations;Pang;Neurosurgery,1993

5. Involvement of the HLXB9 homeobox gene in Currarino syndrome;Belloni;Am J Hum Genet,2000

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