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Results 1 - 10 of 59 for Evans syndrome
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  1. ... combination of hemolytic anemia and thrombocytopenia, also called Evans syndrome. People with this classic form of ALPS generally ...
  2. ... available. Citation on PubMed Wenger T, Miller D, Evans K. FGFR Craniosynostosis Syndromes Overview. 1998 Oct 20 [updated 2020 Apr 30]. ...
  3. ... 10.1002/ajmg.a.33139. Citation on PubMed Evans DG. Nevoid Basal Cell Carcinoma Syndrome. 2002 Jun 20 [updated 2024 Feb 22]. In: ... Cheesman E, Kelsey A, McCabe MG, Newman WG, Evans DG. Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated ...
  4. ... 037. Citation on PubMed Wenger T, Miller D, Evans K. FGFR Craniosynostosis Syndromes Overview. 1998 Oct 20 [updated 2020 Apr 30]. ...
  5. ... x. Citation on PubMed Wenger T, Miller D, Evans K. FGFR Craniosynostosis Syndromes Overview. 1998 Oct 20 [updated 2020 Apr 30]. ...
  6. ... 0387. Citation on PubMed Wenger T, Miller D, Evans K. FGFR Craniosynostosis Syndromes Overview. 1998 Oct 20 [updated 2020 Apr 30]. ...
  7. ... 0387. Citation on PubMed Wenger T, Miller D, Evans K. FGFR Craniosynostosis Syndromes Overview. 1998 Oct 20 [updated 2020 Apr 30]. ...
  8. ... 451. Citation on PubMed Wenger T, Miller D, Evans K. FGFR Craniosynostosis Syndromes Overview. 1998 Oct 20 [updated 2020 Apr 30]. ...
  9. ... NORD) BASAL CELL NEVUS SYNDROME 1; BCNS1 PubMed Evans DG. Nevoid Basal Cell Carcinoma Syndrome. 2002 Jun 20 [updated 2024 Feb 22]. In: ...
  10. ... syndrome National Organization for Rare Disorders (NORD) WINCHESTER SYNDROME; WNCHRS PubMed Evans BR, Mosig RA, Lobl M, Martignetti CR, Camacho C, Grum-Tokars V, Glucksman MJ, Martignetti JA. Mutation of membrane type-1 ... and arthritis disease Winchester syndrome. Am J Hum Genet. 2012 Sep 7;91( ...
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