Literature DB >> 10804739

Three patients with different phenotypes in a family with chromosome 22q11.2 deletions.

T Akiba1, A Odake, E Shirahata, A Matsunaga, M Sakamoto, N Yazaki.   

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Year:  2000        PMID: 10804739     DOI: 10.1046/j.1442-200x.2000.01183.x

Source DB:  PubMed          Journal:  Pediatr Int        ISSN: 1328-8067            Impact factor:   1.524


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  1 in total

1.  Congenital asymmetric crying facies syndrome: A case report.

Authors:  Xiaoqiu Liang; Birong He
Journal:  Medicine (Baltimore)       Date:  2018-08       Impact factor: 1.817

  1 in total

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