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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2004 | 2 |
2007 | 1 |
2012 | 1 |
2013 | 1 |
2024 | 0 |
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Page 1
Deletion 16p13.11 uncovers NDE1 mutations on the non-deleted homolog and extends the spectrum of severe microcephaly to include fetal brain disruption.
Am J Med Genet A. 2013 Jul;161A(7):1523-30. doi: 10.1002/ajmg.a.35969. Epub 2013 May 23.
Am J Med Genet A. 2013.
PMID: 23704059
Free PMC article.
A homozygous IER3IP1 mutation causes microcephaly with simplified gyral pattern, epilepsy, and permanent neonatal diabetes syndrome (MEDS).
Abdel-Salam GM, Schaffer AE, Zaki MS, Dixon-Salazar T, Mostafa IS, Afifi HH, Gleeson JG.
Abdel-Salam GM, et al.
Am J Med Genet A. 2012 Nov;158A(11):2788-96. doi: 10.1002/ajmg.a.35583. Epub 2012 Sep 18.
Am J Med Genet A. 2012.
PMID: 22991235
Free PMC article.
Item in Clipboard
Identification of a novel recessive RELN mutation using a homozygous balanced reciprocal translocation.
Zaki M, Shehab M, El-Aleem AA, Abdel-Salam G, Koeller HB, Ilkin Y, Ross ME, Dobyns WB, Gleeson JG.
Zaki M, et al.
Am J Med Genet A. 2007 May 1;143A(9):939-44. doi: 10.1002/ajmg.a.31667.
Am J Med Genet A. 2007.
PMID: 17431900
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Lis1 and doublecortin function with dynein to mediate coupling of the nucleus to the centrosome in neuronal migration.
Tanaka T, Serneo FF, Higgins C, Gambello MJ, Wynshaw-Boris A, Gleeson JG.
Tanaka T, et al.
J Cell Biol. 2004 Jun 7;165(5):709-21. doi: 10.1083/jcb.200309025. Epub 2004 Jun 1.
J Cell Biol. 2004.
PMID: 15173193
Free PMC article.
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Cytoskeletal-associated proteins in the migration of cortical neurons.
Bielas SL, Gleeson JG.
Bielas SL, et al.
J Neurobiol. 2004 Jan;58(1):149-59. doi: 10.1002/neu.10280.
J Neurobiol. 2004.
PMID: 14598377
Review.
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