Literature DB >> 24817670

Response to "De novo mutation of the TGFB3 latency-associated peptide domain in a patient with overgrowth and Loeys-Dietz syndrome features".

Hugh Young Rienhoff1.   

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Year:  2014        PMID: 24817670     DOI: 10.1002/ajmg.a.36603

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


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  2 in total

1.  Mutations in a TGF-β ligand, TGFB3, cause syndromic aortic aneurysms and dissections.

Authors:  Aida M Bertoli-Avella; Elisabeth Gillis; Hiroko Morisaki; Judith M A Verhagen; Bianca M de Graaf; Gerarda van de Beek; Elena Gallo; Boudewijn P T Kruithof; Hanka Venselaar; Loretha A Myers; Steven Laga; Alexander J Doyle; Gretchen Oswald; Gert W A van Cappellen; Itaru Yamanaka; Robert M van der Helm; Berna Beverloo; Annelies de Klein; Luba Pardo; Martin Lammens; Christina Evers; Koenraad Devriendt; Michiel Dumoulein; Janneke Timmermans; Hennie T Bruggenwirth; Frans Verheijen; Inez Rodrigus; Gareth Baynam; Marlies Kempers; Johan Saenen; Emeline M Van Craenenbroeck; Kenji Minatoya; Ritsu Matsukawa; Takuro Tsukube; Noriaki Kubo; Robert Hofstra; Marie Jose Goumans; Jos A Bekkers; Jolien W Roos-Hesselink; Ingrid M B H van de Laar; Harry C Dietz; Lut Van Laer; Takayuki Morisaki; Marja W Wessels; Bart L Loeys
Journal:  J Am Coll Cardiol       Date:  2015-04-07       Impact factor: 24.094

2.  Reflections on my daughter's DNA.

Authors:  Hugh Young Rienhoff
Journal:  Appl Transl Genom       Date:  2016-02-01
  2 in total

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