These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
141 related articles for article (PubMed ID: 2585460)
1. Familial mental retardation associated with balanced chromosome rearrangement rcp t(8;11)(q24.3;p15.1). Sato H; Takaya K; Nihira S; Fujita H J Med Genet; 1989 Oct; 26(10):642-4. PubMed ID: 2585460 [TBL] [Abstract][Full Text] [Related]
2. A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24). Balci S; Aypar E; Beksaç MS; Bartsch O Genet Couns; 2009; 20(2):125-32. PubMed ID: 19650409 [TBL] [Abstract][Full Text] [Related]
3. Coexistence of Fragile-X Syndrome, 8p23.1 Deletion, and Balanced Translocation t(7;10)(p10;q24) in a Single Family. Cortés H; Reyes-Rosales M; Rojas-Velasco AJ; García-Juárez B; Tapia-Guerrero YS; Arenas-Diaz S; Leyva-García N; Macías-Gallardo JJ; Carrillo-Mora P; Magaña JJ Genet Test Mol Biomarkers; 2020 Aug; 24(8):527-531. PubMed ID: 32716213 [No Abstract] [Full Text] [Related]
4. Aniridia, mental retardation and an unbalanced reciprocal translocation of chromosomes 8 and 11 with an interstitial deletion of 11p. Gödde-Salz E; Behnke H Eur J Pediatr; 1981 Mar; 136(1):93-6. PubMed ID: 7215394 [TBL] [Abstract][Full Text] [Related]
5. Mental retardation with 45 chromosomes 45,XX,--5,--14,+der(5) t(5,14)(p15;q13) mat due to familial balanced reciprocal translocation. Fried K; Tieder M; Beer S; Rosenblatt M; Krespin HI J Med Genet; 1977 Feb; 14(1):68-72. PubMed ID: 839506 [TBL] [Abstract][Full Text] [Related]
6. Langer-Giedion syndrome. A patient without mental retardation and a large 8q23.2-q24.22 deletion. Tiberio G; Digilio MC; Giannotti A Minerva Pediatr; 1999; 51(9-10):313-8. PubMed ID: 10783592 [TBL] [Abstract][Full Text] [Related]
7. Two cases of partial trisomy 8p and partial monosomy 21q in a family with a reciprocal translocation (8;21)(p21.1;q22.3). Plomp AS; Engelen JJ; Albrechts JC; de Die-Smulders CE; Hamers AJ J Med Genet; 1998 Jul; 35(7):604-8. PubMed ID: 9678708 [TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1. Chen CP; Lin MH; Chen YY; Chern SR; Chen YN; Wu PS; Pan CW; Lee MS; Wang W Taiwan J Obstet Gynecol; 2015 Oct; 54(5):592-6. PubMed ID: 26522117 [TBL] [Abstract][Full Text] [Related]
9. Third case of 8q23.3-q24.13 deletion in a patient with Langer-Giedion syndrome phenotype without TRPS1 gene deletion. Pereza N; Severinski S; Ostojić S; Volk M; Maver A; Dekanić KB; Kapović M; Peterlin B Am J Med Genet A; 2012 Mar; 158A(3):659-63. PubMed ID: 22315192 [TBL] [Abstract][Full Text] [Related]
10. Unusual chromosomal mosaicism as a cause of mental retardation and congenital malformations in a familial reciprocal translocation carrier, t(17;22)(q24.2;q11.23). Dufke A; Mayrhofer H; Enders H; Kaiser P; Leipoldt M Cytogenet Cell Genet; 2001; 93(3-4):168-70. PubMed ID: 11528107 [TBL] [Abstract][Full Text] [Related]
11. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y. Delicado A; Lapunzina P; Palomares M; Molina MA; Galán E; López Pajares I Eur J Med Genet; 2005; 48(2):159-66. PubMed ID: 16053907 [TBL] [Abstract][Full Text] [Related]
12. Novel chromosomal translocation t(11;9)(p15;p23) involving deletion and duplication of 9p in a girl associated with autism and mental retardation. Yang Y; Wang C; Wang F; Zhu L; Liu H; He X Gene; 2012 Jul; 502(2):154-8. PubMed ID: 22555022 [TBL] [Abstract][Full Text] [Related]
13. Partial deletion 8q without Langer-Giedion syndrome: a recognisable syndrome. Fennell SJ; Benson JW; Kindley AD; Schwarz MJ; Czepulkowski B J Med Genet; 1989 Mar; 26(3):167-71. PubMed ID: 2651669 [TBL] [Abstract][Full Text] [Related]
14. Multiple exostoses in a patient with t(8;11)(q24.11;p15.5). Ogle RF; Dalzell P; Turner G; Wass D; Yip MY J Med Genet; 1991 Dec; 28(12):881-3. PubMed ID: 1757967 [TBL] [Abstract][Full Text] [Related]
15. A 5q12.1-5q12.3 microdeletion in a case with a balanced exceptional complex chromosomal rearrangement. Cetin Z; Yakut S; Clark OA; Mihci E; Berker S; Luleci G Gene; 2013 Mar; 516(1):176-80. PubMed ID: 23262338 [TBL] [Abstract][Full Text] [Related]
16. De novo balanced translocation (2;10)(q24;q22) associated with mental retardation. Santos CB; Discepoli G; Pigliapoco F; Boy R; Pimentel MM Ann Genet; 2003; 46(4):471-3. PubMed ID: 14659784 [TBL] [Abstract][Full Text] [Related]
17. Segregation of an insertional chromosome rearrangement in 3 generations. Toomey KE; Mohandas T; Sparkes RS; Kaback MM; Rimoin DL J Med Genet; 1978 Oct; 15(5):382-7. PubMed ID: 739529 [TBL] [Abstract][Full Text] [Related]
18. Partial monosomy of 7q32 in a case of de novo rcp(7;15)(q32;q15). D'Alessandro E; Ligas C; Lo Re ML; Marcanio MP; Gentile T; Del Porto G J Med Genet; 1994 May; 31(5):413-5. PubMed ID: 8064823 [TBL] [Abstract][Full Text] [Related]
19. A complex rearrangement, including a deleted 8q, in a case of Langer-Giedion syndrome. Schwartz S; Beisel JH; Panny SR; Cohen MM Clin Genet; 1985 Feb; 27(2):175-82. PubMed ID: 3872186 [TBL] [Abstract][Full Text] [Related]