Literature DB >> 29240610

First case of nonalcoholic steatohepatitis in a child with del(1p36) and dup (Xp22): review of the literature.

Valerio Nobili1,2, Antonella Mosca1, Paola Francalanci3, Digilio Maria Cristina4, Bruno Dallapiccola5,4.   

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Year:  2018        PMID: 29240610     DOI: 10.1097/MCD.0000000000000210

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


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  1 in total

1.  Dental anomalies as a possible clue of 1p36 deletion syndrome due to germline mosaicism: a case report.

Authors:  D Nistico'; F Guidolin; C O Navarra; M Bobbo; A Magnolato; A P D'Adamo; E Giorgio; B Pivetta; E Barbi; P Gasparini; M Cadenaro; F Sirchia
Journal:  BMC Pediatr       Date:  2020-05-09       Impact factor: 2.125

  1 in total

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