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Journal Abstract Search

151 related items for PubMed ID: 26689622

  • 1. Two familial microduplications of 15q26.3 causing overgrowth and variable intellectual disability with normal copy number of IGF1R.
    Leffler M, Puusepp S, Žilina O, Zhu Y, Kuuse K, Bain N, Burgess T, Õunap K, Field M.
    Eur J Med Genet; 2016 Apr; 59(4):257-62. PubMed ID: 26689622
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  • 3. Overgrowth and trisomy 15q26.1-qter including the IGF1 receptor gene: report of two families and review of the literature.
    Faivre L, Gosset P, Cormier-Daire V, Odent S, Amiel J, Giurgea I, Nassogne MC, Pasquier L, Munnich A, Romana S, Prieur M, Vekemans M, De Blois MC, Turleau C.
    Eur J Hum Genet; 2002 Nov; 10(11):699-706. PubMed ID: 12404101
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  • 4. Case of 15q26-qter deletion associated with a Prader-Willi phenotype.
    Santos JFD, Acosta AX, Scheibler GG, Pitanga PML, Alves ES, Meira JGC, Zanardo ÉA, Kulikowski LD, Lima RLLF, Carvalho AFL.
    Eur J Med Genet; 2020 Aug; 63(8):103955. PubMed ID: 32473228
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  • 5. Variable behavioural phenotypes of patients with monosomies of 15q26 and a review of 16 cases.
    Poot M, Verrijn Stuart AA, van Daalen E, van Iperen A, van Binsbergen E, Hochstenbach R.
    Eur J Med Genet; 2013 Jul; 56(7):346-50. PubMed ID: 23603061
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  • 7. Phenotype-genotype correlation in a familial IGF1R microdeletion case.
    Veenma DC, Eussen HJ, Govaerts LC, de Kort SW, Odink RJ, Wouters CH, Hokken-Koelega AC, de Klein A.
    J Med Genet; 2010 Jul; 47(7):492-8. PubMed ID: 19955558
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  • 10. 15q26 deletion in a patient with congenital heart defect, growth restriction and intellectual disability: case report and literature review.
    Benbouchta Y, De Leeuw N, Amasdl S, Sbiti A, Smeets D, Sadki K, Sefiani A.
    Ital J Pediatr; 2021 Sep 16; 47(1):188. PubMed ID: 34530895
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  • 11. Hemizygosity at the insulin-like growth factor I receptor (IGF1R) locus and growth failure in the ring chromosome 15 syndrome.
    Peoples R, Milatovich A, Francke U.
    Cytogenet Cell Genet; 1995 Sep 16; 70(3-4):228-34. PubMed ID: 7789178
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  • 12. Tall stature and duplication of the insulin-like growth factor I receptor gene.
    Kant SG, Kriek M, Walenkamp MJ, Hansson KB, van Rhijn A, Clayton-Smith J, Wit JM, Breuning MH.
    Eur J Med Genet; 2007 Sep 16; 50(1):1-10. PubMed ID: 17056309
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  • 14. Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization, and perinatal findings in a fetus with dup(15)(q26.2q26.3).
    Chen CP, Lin YH, Au HK, Su YN, Hsu CY, Liu YP, Wu PC, Chern SR, Chen YT, Chen LF, Hsieh AH, Wang W.
    Taiwan J Obstet Gynecol; 2011 Sep 16; 50(3):359-65. PubMed ID: 22030053
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  • 15. A girl with 15q overgrowth syndrome and dup(15)(q24q26.3) that included telomeric sequences.
    Gutiérrez-Franco Mde L, Madariaga-Campos Mde L, Vásquez-Velásquez AI, Matute E, Guevara-Yáñez R, Rivera H.
    Korean J Lab Med; 2010 Jun 16; 30(3):318-24. PubMed ID: 20603595
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  • 16. Acute leukemia in a patient with 15q overgrowth syndrome.
    Bodle EE, Gupta R, Cherry AM, Muffly L, Manning MA.
    Am J Med Genet A; 2019 Jun 16; 179(6):1025-1029. PubMed ID: 30861314
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  • 19. [A case of partial trisomy 15q25.3-qter].
    Kim JH, Lee WM, Ryoo NH, Ha JS, Jeon DS, Kim JR, Kim JS, Lee SY.
    Korean J Lab Med; 2009 Feb 16; 29(1):66-70. PubMed ID: 19262081
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