1 Ocak 2011 Dergi makalesi Açık Erişim

Hanna, R. M.; Marsh, S. E.; Swistun, D.; Al-Gazali, L.; Zaki, M. S.; Abdel-Salam, G. M.; Al-Tawari, A.; Bastaki, L.; Kayserili, H.; Rajab, A.; Boglarka, B.; Dietrich, R. B.; Dobyns, W. B.; Truwit, C. L.; Sattar, S.; Chuang, N. A.; Sherr, E. H.; Gleeson, J. G.

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  "@context": "https://schema.org/", 
  "@id": 19477, 
  "@type": "ScholarlyArticle", 
  "creator": [
    {
      "@type": "Person", 
      "affiliation": "Rady Childrens Hosp, Howard Hughes Med Inst, Dept Neurosci & Pediat, San Diego, CA USA", 
      "name": "Hanna, R. M."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Rady Childrens Hosp, Howard Hughes Med Inst, Dept Neurosci & Pediat, San Diego, CA USA", 
      "name": "Marsh, S. E."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Rady Childrens Hosp, Howard Hughes Med Inst, Dept Neurosci & Pediat, San Diego, CA USA", 
      "name": "Swistun, D."
    }, 
    {
      "@type": "Person", 
      "affiliation": "United Arab Emirates Univ, Fac Med & Hlth Sci, Dept Paediat, Al Ain, U Arab Emirates", 
      "name": "Al-Gazali, L."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Natl Res Ctr, Dept Clin Genet, Human Genet & Genome Res Div, Cairo, Egypt", 
      "name": "Zaki, M. S."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Natl Res Ctr, Dept Clin Genet, Human Genet & Genome Res Div, Cairo, Egypt", 
      "name": "Abdel-Salam, G. M."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Al Sabah Hosp, Pediat Neurol Unit, Kuwait, Kuwait", 
      "name": "Al-Tawari, A."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Kuwait Med Genet Ctr, Kuwait, Kuwait", 
      "name": "Bastaki, L."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Istanbul Univ, Istanbul Fac Med, Dept Med Genet, Istanbul, Turkey", 
      "name": "Kayserili, H."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Minist Hlth, Genet Unit, Muscat, Oman", 
      "name": "Rajab, A."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Semmelweis Univ, Dept Pediat, Budapest, Hungary", 
      "name": "Boglarka, B."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Univ Calif San Diego, Dept Radiol, La Jolla, CA 92093 USA", 
      "name": "Dietrich, R. B."
    }, 
    {
      "@type": "Person", 
      "name": "Dobyns, W. B."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Univ Minnesota, Sch Med, Dept Radiol Neuroradiol & Magnet Resonance, Minneapolis, MN 55455 USA", 
      "name": "Truwit, C. L."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Rady Childrens Hosp, Howard Hughes Med Inst, Dept Neurosci & Pediat, San Diego, CA USA", 
      "name": "Sattar, S."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Rady Childrens Hosp, San Diego Imaging Med Grp, Neuroradiol Div, San Diego, CA USA", 
      "name": "Chuang, N. A."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA", 
      "name": "Sherr, E. H."
    }, 
    {
      "@type": "Person", 
      "affiliation": "Rady Childrens Hosp, Howard Hughes Med Inst, Dept Neurosci & Pediat, San Diego, CA USA", 
      "name": "Gleeson, J. G."
    }
  ], 
  "datePublished": "2011-01-01", 
  "description": "Objective: We sought to create a classification system for pediatric corpus callosal abnormalities (CCA) based upon midline sagittal brain MRI. We used the term CCA for patients with structural variants of the corpus callosum, excluding patients with interhemispheric cyst variant or pure dysplasia without hypoplasia. Currently, no system exists for nonsyndromic forms of CCA, and attempts to create such a system have been hampered by highly variable morphology in patients with sporadic CCA. We reasoned that any useful strategy should classify affected family members within the same type, and that phenotypic variability should be minimized in patients with recessive disease.", 
  "headline": "Distinguishing 3 classes of corpus callosal abnormalities in consanguineous families", 
  "identifier": 19477, 
  "image": "https://aperta.ulakbim.gov.tr/static/img/logo/aperta_logo_with_icon.svg", 
  "license": "http://www.opendefinition.org/licenses/cc-by", 
  "name": "Distinguishing 3 classes of corpus callosal abnormalities in consanguineous families", 
  "url": "https://aperta.ulakbim.gov.tr/record/19477"
}