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Results 1 - 10 of 71 for robert syndrome 26
  1. ... 37657. Epub 2016 Apr 25. Citation on PubMed Roberts AE, Allanson JE, Tartaglia M, Gelb BD. Noonan syndrome. Lancet. 2013 Jan 26;381(9863):333-42. doi: 10.1016/S0140- ...
  2. ... Inactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome: no ... 2006 Apr 18 [updated 2020 Mar 26]. In: Adam MP, Feldman J, Mirzaa GM, Pagon ...
  3. ... Inactivating mutations in ESCO2 cause SC phocomelia and Roberts syndrome: no ... 2006 Apr 18 [updated 2020 Mar 26]. In: Adam MP, Feldman J, Mirzaa GM, Pagon ...
  4. ... RM, Castillo-Mosquera N, Nuttall EA, Paul A, Roberts CA, Solomonidis EG, ... syndrome. Blood. 2016 Jun 30;127(26):3387-97. doi: 10.1182/blood-2016-02- ...
  5. ... Londono R, Pepin M, Pope FM, Reinstein E, Robert L, Rohrbach M, Sanders L, ... Med Genet. 2017 Mar;175(1):8-26. doi: 10.1002/ajmg.c.31552. Citation on ...
  6. ... Londono R, Pepin M, Pope FM, Reinstein E, Robert L, Rohrbach M, Sanders L, ... Med Genet. 2017 Mar;175(1):8-26. doi: 10.1002/ajmg.c.31552. Citation on ...
  7. ... Londono R, Pepin M, Pope FM, Reinstein E, Robert L, Rohrbach M, Sanders L, ... Med Genet. 2017 Mar;175(1):8-26. doi: 10.1002/ajmg.c.31552. Citation on ...
  8. ... Londono R, Pepin M, Pope FM, Reinstein E, Robert L, Rohrbach M, Sanders L, ... Med Genet. 2017 Mar;175(1):8-26. doi: 10.1002/ajmg.c.31552. Citation on ...
  9. ... Londono R, Pepin M, Pope FM, Reinstein E, Robert L, Rohrbach M, Sanders L, ... Med Genet. 2017 Mar;175(1):8-26. doi: 10.1002/ajmg.c.31552. Citation on ...
  10. ... Londono R, Pepin M, Pope FM, Reinstein E, Robert L, Rohrbach M, Sanders L, ... Med Genet. 2017 Mar;175(1):8-26. doi: 10.1002/ajmg.c.31552. Citation on ...
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