Literature DB >> 30378271

Myelodysplastic syndrome with multilineage dysplasia evolving to acute myeloid leukemia: Noonan syndrome with c.218C>T mutation in PTPN11 gene.

Rathika Damodara Shenoy1, Sunil Kumar Yeshvanth2, Harsha Prasada L3, Vijaya Shenoy1, Vikram Shetty4.   

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Year:  2018        PMID： 30378271     DOI： 10.1002/pbc.27527

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN： 1545-5009            Impact factor:   3.167


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  1 in total

1.  Rapid detection by hydrops panel of Noonan syndrome with PTPN11 mutation (p.Thr73Ile) and persistent thrombocytopenia.

Authors:  Mascha Schönfeld; Mareike Selig; Alexandra Russo; Christine Lindner; Christoph Kampmann; Eva Mildenberger; Catharina Whybra
Journal:  Mol Genet Genomic Med       Date:  2020-03-07       Impact factor: 2.183
  1 in total

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