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Results 1 - 10 of 660 for Robert
  1. Roberts syndrome is a genetic disorder characterized by limb and facial abnormalities. Affected individuals also grow slowly before and after birth. Mild to ...
  2. ... LIS3 Lissencephaly 2 Lissencephaly 3 Lissencephaly syndrome, Norman-Roberts type Norman-Roberts syndrome Genetic Testing Registry: Lissencephaly type 3 Genetic ...
  3. Thalassemia: Complications and Treatment (Centers for Disease Control and Prevention)  
    Thalassemia/Treatments and Therapies ... Thalassemia ... Centers for Disease Control and Prevention ... If I have thalassemia, how does it affect my body? Since your ...
  4. Healthy Living with Thalassemia (Centers for Disease Control and Prevention)  
    Thalassemia/Living With ... Thalassemia ... Centers for Disease Control and Prevention ... A healthy lifestyle is important for everyone. For people living with thalassemia, ...
  5. ... Eye Institute National Institutes of Health Bethesda, Maryland Robert Arceci Johns Hopkins University Baltimore, Maryland Kathleen Arnos ... Bertini Bambino Gesu Children’s Research Hospital Rome, Italy Robert Best University of South Carolina Columbia, South Carolina ...
  6. ... ESCO2 gene mutations have been found to cause Roberts syndrome, which is characterized by limb and facial ... around the chromosome's constriction point (centromere). In Roberts syndrome, cells respond to abnormal sister chromatid attachment ...
  7. ... Morgan MB, Muzny DM, Stein L, McPherson JD, Roberts AE, Gibbs RA, Neel BG, Kucherlapati R. Next- ... Zenker M, Zampino G, Verloes A, Dallapiccola B, Roberts AE, Cave H, Gelb BD, Neel BG, Tartaglia ...
  8. ... A, Furin M, Overberger R. Prehospital immobilization. In: Roberts JR, Custalow CB, Thomsen TW, eds. Roberts and Hedges' Clinical Procedures in Emergency Medicine and ...
  9. ... article on PubMed Central Sarvananthan N, Surendran M, Roberts EO, Jain S, Thomas S, Shah N, Proudlock ... Sarvananthan N, Mallya U, Lisgo S, Talbot CJ, Roberts EO, Awan M, Surendran M, McLean RJ, Reinecke ...
  10. ... MICROCEPHALY-ASSOCIATED; ASPM NCBI Gene ClinVar Bond J, Roberts E, Mochida GH, Hampshire DJ, Scott S, Askham ... Jafri H, Rashid Y, Mubaidin A, Walsh CA, Roberts E, Woods CG. Protein-truncating mutations in ASPM ...
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