Literature DB >> 9301367

Chromosomal and clinical features in an infant with Hallermann-Streiff syndrome.

G F Pugliese, G Latorre, F Latorre.   

Abstract

Entities:  

Mesh：

Year:  1997        PMID： 9301367      PMCID： PMC1717296          DOI： 10.1136/adc.77.2.183b

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


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  2 in total

1.  Hallermann-Streiff syndrome with severe bilateral enophthalmos and radiological evidence of silent brain syndrome: a new congenital silent brain syndrome?

Authors:  Paolo Nucci; Carlo de Conciliis; Matteo Sacchi; Massimiliano Serafino
Journal:  Clin Ophthalmol       Date:  2011-07-04

2.  Hallermann-Streiff syndrome with uncommon ocular features, ultrasound biomicroscopy and optical coherence tomography findings: A case report.

Authors:  Wei Shen; Min Dai; Yunshan Su; Qing Zhang; Hongsong Li
Journal:  Medicine (Baltimore)       Date:  2019-12       Impact factor: 1.889
  2 in total

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