Meeting Abstract, 2024

Ritscher-Schinzel syndrome: broadening the phenotype in prenatal and adulthood

EUROPEAN JOURNAL OF HUMAN GENETICS, ISSN 1018-4813, Volume 32, Page 538,

Contributors

Nery, Sabrina [1] [2] Maia, Nuno 0000-0003-3274-2474 [3] [4] Fortuna, Ana Maria [3] [4] [5] Damasio, Joana [3] [4] [5] [6] COALE, E [7] [8] Willisi, Mary [9] [10] [11] Jorge, Paula [3] [4] [5] Hojte, Anne F. [2] Fenger, Christina Duhring [2] [12] Moeller, Rikke Steensbjerre [2] [13] Bayat, Allan 0000-0003-4986-8006 [2] [13]

Affiliations

  1. [1] Magna Graecia Univ Catanzaro, Dept Med & Surg Sci, Catanzaro, Italy
    2. [NORA names: Italy; Europe, EU; OECD];
  2. [2] Danish Epilepsy Ctr, Dept Epilepsy Genet & Personalized Med, Dianalund, Denmark
    3. [NORA names: Filadelfia - Danish Epilepsy Hospital; Hospital; Denmark; Europe, EU; Nordic; OECD];
  3. [3] Ctr Hosp Univ Santo Antonio CHUdSA, Ctr Genet Med Jacinto Magalhaes CGM, Porto, Portugal
    4. [NORA names: Portugal; Europe, EU; OECD];
  4. [4] Univ Porto, ICBAS Sch Med & Biomed Sci, UMIB Unit Multidisciplinary Res Biomed, Porto, Portugal
    5. [NORA names: Portugal; Europe, EU; OECD];
  5. [5] ITR Lab Integrat & Translat Res Populat Hlth, Porto, Portugal
    6. [NORA names: Portugal; Europe, EU; OECD];

Data Provider: Clarivate

LINKS
-

Matching Records in NORA

  • No Matches Found

SUBJECTS
+

METRICS
+