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Kroes HY, Tuerlings JH, Hordijk R, et al. 
Another patient with an interstitial deletion of chromosome 9: case report and a review of six cases with del(9)(q22q32). [Journal Article, Review]
J Med Genet 1994 Feb; 31(2):156-8.
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Prasher VP, Krishnan VH, Clarke DJ, et al. 
Deletion of chromosome 2 (p11-p13): case report and review. [Case Reports, Journal Article, Review]
J Med Genet 1993 Jul; 30(7):604-6.
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Beemer FA, Klep-de Pater JM, Sepers GJ, et al. 
Two cases of interstitial deletion of the long arm of chromosome 1: del(1)(q21----q25) and del(1)(q41----q43). [Case Reports, Journal Article]
Clin Genet 1985 May; 27(5):515-9.
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Copelli S, del Rey G, Heinrich J, et al. 
Brief clinical report: interstitial deletion of the long arm of chromosome 4, del(4)(q28-->q31.3). [Case Reports, Journal Article]
Am J Med Genet 1995 Jan 2; 55(1):77-9.
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Larson SA, Yeatman GW, Riccardi VM 
Deletion of 11q: report of two cases and a review. [Case Reports, Journal Article]
Birth Defects Orig Artic Ser 1976; 12(5):125-30.
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Maranda B, Lemieux N, Lemyre E 
Familial deletion 18p syndrome: Case report. [JOURNAL ARTICLE]
BMC Med Genet 2006 Jul 14; 7(1):60.
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Mowat DR, Croaker GD, Cass DT, et al. 
Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23. [Case Reports, Journal Article]
J Med Genet 1998 Aug; 35(8):617-23.
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Taysi K, Dengler DR, Jones LA, et al. 
Interstitial deletion of the long arm of chromosome 2: case report and review of literature. [Case Reports, Journal Article, Review]
Ann Genet 1981; 24(4):245-7.
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Wilson MG, Towner JW, Forsman I, et al. 
Syndromes associated with deletion of the long arm of chromosome 18[del(18q)]. [Case Reports, Journal Article]
Am J Med Genet 1979; 3(2):155-74.
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