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Results 1 - 10 of 76 for fd
  1. Familial dysautonomia (FD) is an inherited disorder that affects nerves throughout the body. ... FD is passed down through families (inherited). A person must inherit a copy of the defective gene ...
  2. ... not show signs and symptoms of the condition. FD HSAN type III HSAN3 HSN-III Riley-Day ...
  3. Hereditary hemochromatosis is a disorder that causes the body to absorb too much iron from the diet. The excess iron is stored in the body's tissues and organs, ...
  4. ... AG, Moore AT, Keefe RO, Black GC, Manson FD. ADVIRC is caused by distinct mutations in BEST1 ... GA, Kestelyn P, Holder GE, Webster AR, Manson FD, Black GC. Biallelic mutation of BEST1 causes a ...
  5. ... ClinVar Bianconi SE, Cross JL, Wassif CA, Porter FD. Pathogenesis, Epidemiology, Diagnosis and Clinical Aspects of Smith- ... article on PubMed Central Correa-Cerro LS, Porter FD. 3beta-hydroxysterol Delta7-reductase and the Smith-Lemli- ...
  6. Is It a Cosmetic, a Drug, or Both? (or Is It Soap?) (Food and Drug Administration)  
    Cosmetics/Start Here ... Cosmetics ... Food and Drug Administration ... An overview of the legal differences between cosmetics and drugs, and whether a cosmetic can ...
  7. Fibrous Dysplasia/McCune-Albright Syndrome From the National Institutes of Health (National Institute of Dental and Craniofacial Research)  
    Bone Diseases/Specifics ... Bone Diseases ... National Institute of Dental and Craniofacial Research ... From the National Institutes of Health
  8. Does the Product Emit Radiation? (Food and Drug Administration)  
    Radiation Exposure/Start Here ... Radiation Exposure ... Food and Drug Administration ... Information about radiation-emitting products, including determination and ...
  9. ... A, Tamiazzo S, Provera S, Pierluigi M, Bricarelli FD. The natural history of Cri du Chat Syndrome. ... S, Zara F, Overhauser J, Pierluigi M, Bricarelli FD. Clinical and molecular characterisation of 80 patients with ...
  10. ... AG, Moore AT, Keefe RO, Black GC, Manson FD. ADVIRC is caused by distinct mutations in BEST1 ... JJ, Puech B, Kestelyn P, Moore AT, Manson FD, Black GC. Mutations of VMD2 splicing regulators cause ...
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