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15 results
  1. ... see-reference >Reactive Arthritis</see-reference><see-reference >Reiter's Syndrome</see-reference><see-reference >Septic Arthritis</see-reference><site ><information- ...
  2. ... and Diseases from OMIM CHROMOSOME 15q11-q13 DUPLICATION SYNDROME Scientific Articles on PubMed PubMed References Battaglia A, Bernardini L, Torrente I, Novelli A, ...
  3. ... of Genes and Diseases from OMIM SMITH-MAGENIS SYNDROME; SMS Scientific Articles on PubMed PubMed References Carmona-Mora P, Encina CA, Canales CP, Cao ...
  4. ... Catalog of Genes and Diseases from OMIM HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC; HES Scientific Articles on PubMed PubMed References Buitenhuis M, Verhagen LP, Cools J, Coffer PJ. ...
  5. ... and Diseases from OMIM CHROMOSOME Xq26.3 DUPLICATION SYNDROME Scientific Articles on PubMed PubMed References Beckers A, Lodish MB, Trivellin G, Rostomyan L, ...
  6. ... PDGFRA Gene and Variant Databases NCBI Gene ClinVar References Bain BJ. Relationship between idiopathic hypereosinophilic syndrome, eosinophilic leukemia, and systemic mastocytosis. Am J Hematol. ...
  7. ... 2007 Nov 22. Citation on PubMed Macdonald D, Reiter A, Cross NC. The 8p11 myeloproliferative syndrome: a distinct clinical entity caused by constitutive activation ...
  8. ... BETA; PDGFRB MYOFIBROMATOSIS, INFANTILE, 1; IMF1 KOSAKI OVERGROWTH SYNDROME; KOGS Gene and Variant Databases NCBI Gene ClinVar References Apperley JF, Gardembas M, Melo JV, Russell-Jones ...
  9. ... PubMed Cornish K, Bramble D. Cri du chat syndrome: genotype-phenotype ... NC, Reiter A. Fibroblast growth factor receptor and platelet-derived ...
  10. ... disturbances, hypotonia, intellectual disability, neurologic disorder, and epilepsy syndrome ... References Levy AM, Gomez-Puertas P, Tumer Z. Neurodevelopmental ...
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