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Connection

William Dobyns to Tomography, X-Ray Computed

This is a "connection" page, showing publications William Dobyns has written about Tomography, X-Ray Computed.
Connection Strength

0.239
  1. Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation. Am J Med Genet A. 2006 Nov 15; 140(22):2416-25.
    View in: PubMed
    Score: 0.035
  2. Flores hominid: new species or microcephalic dwarf? Anat Rec A Discov Mol Cell Evol Biol. 2006 Nov; 288(11):1123-45.
    View in: PubMed
    Score: 0.035
  3. MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis. Brain. 2020 01 01; 143(1):55-68.
    View in: PubMed
    Score: 0.022
  4. Walker-Warburg syndrome and tectocerebellar dysraphia: A novel association caused by a homozygous DAG1 mutation. Eur J Paediatr Neurol. 2018 May; 22(3):525-531.
    View in: PubMed
    Score: 0.019
  5. Cobblestone lissencephaly with normal eyes and muscle. Neuropediatrics. 1996 Apr; 27(2):70-5.
    View in: PubMed
    Score: 0.017
  6. Causal heterogeneity in isolated lissencephaly. Neurology. 1992 Jul; 42(7):1375-88.
    View in: PubMed
    Score: 0.013
  7. Clinical and molecular diagnosis of Miller-Dieker syndrome. Am J Hum Genet. 1991 Mar; 48(3):584-94.
    View in: PubMed
    Score: 0.012
  8. Vascular abnormalities in epidermal nevus syndrome. Neurology. 1991 Feb; 41(2 ( Pt 1)):276-8.
    View in: PubMed
    Score: 0.012
  9. Agenesis of the corpus callosum and gyral malformations are frequent manifestations of nonketotic hyperglycinemia. Neurology. 1989 Jun; 39(6):817-20.
    View in: PubMed
    Score: 0.011
  10. The neurogenetics of lissencephaly. Neurol Clin. 1989 Feb; 7(1):89-105.
    View in: PubMed
    Score: 0.010
  11. Band-like intracranial calcification with simplified gyration and polymicrogyria: a distinct "pseudo-TORCH" phenotype. Am J Med Genet A. 2008 Dec 15; 146A(24):3173-80.
    View in: PubMed
    Score: 0.010
  12. Megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus (MPPH): report of a new case. Neuropediatrics. 2007 Aug; 38(4):200-3.
    View in: PubMed
    Score: 0.009
  13. Developmental aspects of lissencephaly and the lissencephaly syndromes. Birth Defects Orig Artic Ser. 1987; 23(1):225-41.
    View in: PubMed
    Score: 0.009
  14. Computed tomographic appearance of lissencephaly syndromes. AJNR Am J Neuroradiol. 1985 Jul-Aug; 6(4):545-50.
    View in: PubMed
    Score: 0.008
  15. Periventricular nodular heterotopia in patients with filamin-1 gene mutations: neuroimaging findings. Pediatr Radiol. 2000 Nov; 30(11):748-55.
    View in: PubMed
    Score: 0.006
  16. Childhood stroke and lupus anticoagulant. Pediatr Neurol. 1994 Feb; 10(1):54-7.
    View in: PubMed
    Score: 0.004
  17. Clinical manifestations and evaluation of isolated lissencephaly. Childs Nerv Syst. 1993 Nov; 9(7):387-90.
    View in: PubMed
    Score: 0.004
  18. Microdeletions of chromosome 17p13 as a cause of isolated lissencephaly. Am J Hum Genet. 1992 Jan; 50(1):182-9.
    View in: PubMed
    Score: 0.003
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.