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Results 1 - 10 of 650 for robert
  1. Roberts syndrome 
    Roberts syndrome is a genetic disorder characterized by limb and facial abnormalities. Affected individuals also grow slowly before and after birth. Mild to ...
    https://medlineplus.gov/genetics/condition/roberts-syndrome - Genetics
  2. Lissencephaly with cerebellar hypoplasia 
    ... LIS3 Lissencephaly 2 Lissencephaly 3 Lissencephaly syndrome, Norman-Roberts type Norman-Roberts syndrome Genetic Testing Registry: Lissencephaly type 3 Genetic ...
    https://medlineplus.gov/.../lissencephaly-with-cerebellar-hypoplasia - Genetics
  3. Expert reviewers 
    ... 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 ...
    https://medlineplus.gov/about/general/genetics/expertreviewers -
  4. ESCO2 gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/esco2 - Genetics
  5. Noonan syndrome 
    ... 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 ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  6. Dislocation 
    ... A, Furin M, Overberger R. Prehospital immobilization. In: Roberts JR, Custalow CB, Thomsen TW, eds. Roberts and Hedges' Clinical Procedures in Emergency Medicine and ...
    https://medlineplus.gov/ency/article/000014.htm - Medical Encyclopedia
  7. X-linked infantile nystagmus 
    ... 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 ...
    https://medlineplus.gov/.../condition/x-linked-infantile-nystagmus - Genetics
  8. ASPM gene 
    ... 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 ...
    https://medlineplus.gov/genetics/gene/aspm - Genetics
  9. Branchio-oculo-facial syndrome 
    ... on PubMed Milunsky JM, Maher TA, Zhao G, Roberts AE, Stalker HJ, Zori RT, Burch MN, Clemens ... Meschino WS, Mortier GR, Parkash S, Ray CR, Roberts A, Roberts A, Reardon W, Schnur RE, Smith ...
    https://medlineplus.gov/.../condition/branchio-oculo-facial-syndrome - Genetics
  10. PRKAG2 gene 
    ... Lozado R, Shah G, Fananapazir L, Bachinski LL, Roberts R. Identification of a gene responsible for familial ... on PubMed Gollob MH, Green MS, Tang AS, Roberts R. PRKAG2 cardiac syndrome: familial ventricular preexcitation, conduction ...
    https://medlineplus.gov/genetics/gene/prkag2 - Genetics
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