Expanding the SHOC2 mutation associated phenotype of noonan syndrome with loose anagen hair: Structural brain anomalies and myelofibrosis

Karen W. Gripp, Dina J. Zand, Laurie Demmer, Carol E. Anderson, William B. Dobyns, Elaine H. Zackai, Elizabeth Denenberg, Kim Jenny, Deborah L. Stabley, Katia Sol-Church
  • American Journal of Medical Genetics Part A, July 2013, Wiley
  • DOI: 10.1002/ajmg.a.36098

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The following have contributed to this page: Dr Karen W Gripp