Bıçağın İki Yüzü: Kromozom 17p11.2 Delesyon ve Duplikasyon Sendromları
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Kaynakça
- 1. Potocki L, Chen KS, Park SS, Osterholm DE, Withers MA, Kimonis V, et al. Molecular mechanism for duplication 17p11.2- the homologous recombination reciprocal of the Smith-Magenis microdeletion. Nat Genet 2000;24:84-87.
- 2. Smith AC, McGavran L, Robinson J, Waldstein G, Macfarlane J, Zonona J, et al. Interstitial deletion of (17) (p11.2p11.2) in nine patients. Am J Med Genet 1986;24:393-414. 3. Slager RE, Newton TL, Vlangos CN, Finucane B, Elsea SH. Mutations in RAI1 associated with Smith-Magenis syndrome. Nat Genet 2003;33(4):466-8.
- 4. Potocki L, Bi W, Treadwell-Deering D, Carvalho CM, Eifert A, Friedman EM, et al. Characterization of Potocki–Lupski syndrome (dup(17)(p11.2p11.2)) and delineation of a dosage-sensitive critical interval that can convey an autism phenotype. Am J Hum Genet 2007; 80:633-49.
- 5. Neira-Fresneda J, Potocki L. Neurodevelopmental disorders associated with abnormal gene dosage: Smith-Magenis and Potocki-Lupski syndromes. J Pediatric Genet 2015;4(3);159-67.
- 6. Elsea SH, Girirajan S. Smith-Magenis syndrome. Eur J Hum Genet 2008;16(4):412-21.
- 7. Magoulas PL, Liu P, Gelowani V, Soler-Alfonso C, Kivuva EC, Lupski JR, et al. Inherited dup (17) (p11.2p11.2): expanding the phenotype of the Potocki-Lupski syndrome. Am J Med Genet 2014;164A(2):500-4.
- 8. Cappuccio G, Vitiello F, Casertano A, Fontana P, Genesio R, Bruzzese D, et al. New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants. Ital J Pediatr 2016;42:39.
- 9. Lupski JR, Stankiewicz P. Genomic disorders: Molecular mechanisms for rearrangements and conveyed phenotypes. PLoS Genet 2005;1(6):e49. DOI:10.1371/journal.pgen.0010049. 10. Ricard G, Molina J, Chrast J, Gu W, Gheldof N, Pradervand S, et al. Phenotypic consequences of copy number variation: insights from Smith-Magenis and Potocki-Lupski syndrome mouse models. PLoS Biol 2010;8(11):e1000543. DOI:10.1371/journal.pbio.1000543.
Ayrıntılar
Birincil Dil
Türkçe
Konular
Sağlık Kurumları Yönetimi
Bölüm
Olgu Sunumu
Yazarlar
Turgay Çokyaman
*
0000-0002-7108-6839
Türkiye
Ülgen Özcan Erdem
0000-0003-0267-0051
Türkiye
Hakan Aylanç
Bu kişi benim
0000-0002-8907-3809
Türkiye
Fatma Sılan
0000-0001-7191-2240
Türkiye
Yayımlanma Tarihi
13 Eylül 2021
Gönderilme Tarihi
23 Haziran 2020
Kabul Tarihi
14 Eylül 2020
Yayımlandığı Sayı
Yıl 2021 Cilt: 43 Sayı: 5