| Hong S, Kang SY, Seong GJ, et al. Multiple ocular abnormalities associated with trisomy 4p. [Journal Article] Ophthalmic Surg Lasers Imaging 2008 Sep-Oct; 39(5):412-4. Abstract | Full Citation | Find Related Articles | | Chen G, Kozell LB, Hitzemann R, et al. Involvement of the limbic basal ganglia in ethanol withdrawal convulsivity in mice is influenced by a chromosome 4 locus. [Journal Article, Research Support, N.I.H., Extramural, Research Support, U.S. Gov't, Non-P.H.S.] J Neurosci 2008 Sep 24; 28(39):9840-9. Abstract | Full Citation | Publisher Full Text | Find Related Articles | | South ST, Whitby H, Maxwell T, et al. Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: Modification of the Wolf-Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith-Wiedemann or Russell-Silver phenotype. [JOURNAL ARTICLE] Am J Med Genet A 2008 Sep 16. Abstract | Full Citation | Find Related Articles | | Korn JM, Kuruvilla FG, McCarroll SA, et al. Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs. [Journal Article, Research Support, Non-U.S. Gov't] Nat Genet 2008 Oct; 40(10):1253-60. Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Kaalund SS, Møller RS, Tészás A, et al. Investigation of 4q-deletion in two unrelated patients using array CGH. [JOURNAL ARTICLE] Am J Med Genet A 2008 Aug 7. Full Citation | Find Related Articles | | Cummings TJ, Dodd LG, Eedes CR, et al. Hereditary benign intraepithelial dyskeratosis: an evaluation of diagnostic cytology. [Evaluation Studies, Journal Article] Arch Pathol Lab Med 2008 Aug; 132(8):1325-8. Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Zollino M, Murdolo M, Neri G The terminal 760 kb region on 4p16 is unlikely to be the critical interval for growth delay in Wolf-Hirschhorn syndrome. [Comment, Letter, Research Support, Non-U.S. Gov't] J Med Genet 2008 Aug; 45(8):544. Full Citation | Find Related Articles | | Shriberg LD, Jakielski KJ, El-Shanti H Breakpoint localization using array-CGH in three siblings with an unbalanced 4q;16q translocation and childhood apraxia of speech (CAS). [JOURNAL ARTICLE] Am J Med Genet A 2008 Jul 31. Abstract | Full Citation | Find Related Articles | | Zenteno JC, Ruiz G, Pérez-Cano HJ, et al. Familial Wolfram syndrome due to compound heterozygosity for two novel WFS1 mutations. [Journal Article] Mol Vis 2008.:1353-7. Abstract | Full Citation | | Abe S, Kameoka J, Fujiwara M, et al. Trisomies 4 and 10 in acute myeloid leukemia: report of a new case. [Letter] Cancer Genet Cytogenet 2008 Aug; 185(1):55-6. Full Citation | Find Related Articles |  |
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