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Results 1 - 10 of 119 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. 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
  4. 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
  5. 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
  6. 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
  7. 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
  8. 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
  9. What are secondary findings from genetic testing?: MedlinePlus Genetics 
    ... and how it can impact their medical care. Robert C. Green MD, MPH, Jonathan S. Berg MD, ... Martin PhD, FACMG, Amy L. McGuire JD, PhD, Robert L. Nussbaum MD, Julianne M. O’Daniel MS, ...
    https://medlineplus.gov/.../understanding/testing/secondaryfindings - Genetics
  10. NRAS gene 
    ... Dvorsky R, Gremer L, Carta C, Horn D, Roberts AE, Lepri F, Merbitz-Zahradnik T, Konig R, ... Dahlgren J, Gelb BD, Hall B, Pierpont ME, Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan ...
    https://medlineplus.gov/genetics/gene/nras - Genetics
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