Literature DB >> 19174127

[Familial 18p syndrome -- a clinical case].

Carla Laranjeira, Ana Fortuna, Ana Teixeira, Natália Teles, Susana Peres.   

Abstract

Mesh：

Year:  2008        PMID： 19174127     DOI： 10.1016/j.anpedi.2008.08.012

Source DB:  PubMed          Journal:  An Pediatr (Barc)        ISSN： 1695-4033            Impact factor:   1.500


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  1 in total

1.  The genotype and phenotype of chromosome 18p deletion syndrome: Case series.

Authors:  Qiujie Jin; Rong Qiang; Bo Cai; Xiaobin Wang; Na Cai; Shuai Zhen; Wen Zhai
Journal:  Medicine (Baltimore)       Date:  2021-05-07       Impact factor: 1.889
  1 in total

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