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Chromosomes, Human, Pair 4 journal articles from PubMed MEDLINE database

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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.
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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.
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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.
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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.
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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.
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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.
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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.
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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.
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