236 related articles for article (PubMed ID: 2477654)
21. [Familial chromosome translocation (1;5;15) as a cause of partial trisomy 1p].
Schürmann M; Wethling H; Niemeyer ML; Schwinger E
Klin Padiatr; 1987; 199(1):27-31. PubMed ID: 2435950
[TBL] [Abstract][Full Text] [Related]
22. The alpha-thalassemia/mental retardation syndromes.
Gibbons RJ; Higgs DR
Medicine (Baltimore); 1996 Mar; 75(2):45-52. PubMed ID: 8606626
[TBL] [Abstract][Full Text] [Related]
23. Cryptic chromosomal rearrangement screening in 30 patients with mental retardation and dysmorphic features.
Rodriguez-Revenga L; Badenas C; Sánchez A; Mallolas J; Carrió A; Pedrinaci S; Barrionuevo JL; Milà M
Clin Genet; 2004 Jan; 65(1):17-23. PubMed ID: 15032970
[TBL] [Abstract][Full Text] [Related]
24. Familial mental retardation syndrome ATR-16 due to an inherited cryptic subtelomeric translocation, t(3;16)(q29;p13.3).
Holinski-Feder E; Reyniers E; Uhrig S; Golla A; Wauters J; Kroisel P; Bossuyt P; Rost I; Jedele K; Zierler H; Schwab S; Wildenauer D; Speicher MR; Willems PJ; Meitinger T; Kooy RF
Am J Hum Genet; 2000 Jan; 66(1):16-25. PubMed ID: 10631133
[TBL] [Abstract][Full Text] [Related]
25. [Clinical and molecular cytogenetic analysis of a family with mental retardation caused by an unbalanced translocation involving chromosomes 3 and 22].
Zhang K; Dong R; Huang Y; Yang Y; Wang Y; Zhang H; Zhang Y; Liu Y; Gai Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):30-34. PubMed ID: 28186589
[TBL] [Abstract][Full Text] [Related]
26. Unbalanced inherited complex chromosome rearrangement involving chromosome 8, 10, 11 and 16 in a patient with congenital malformations and delayed development.
Karmous-Benailly H; Giuliano F; Massol C; Bloch C; De Ricaud D; Lambert JC; Perelman S
Eur J Med Genet; 2006; 49(5):431-8. PubMed ID: 16497571
[TBL] [Abstract][Full Text] [Related]
27. Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation.
Erdogan F; Chen W; Kirchhoff M; Kalscheuer VM; Hultschig C; Müller I; Schulz R; Menzel C; Bryndorf T; Ropers HH; Ullmann R
Cytogenet Genome Res; 2006; 115(3-4):247-53. PubMed ID: 17124407
[TBL] [Abstract][Full Text] [Related]
28. Subtelomeric fish findings in Turkish patients with idiopathic mental retardation.
Tos T; Vurucu S; Karkucak M; Kozan S; Gul D; Akin R
Genet Couns; 2013; 24(3):259-64. PubMed ID: 24341139
[TBL] [Abstract][Full Text] [Related]
29. Analysis of a whole arm translocation between chromosomes 18 and 20 using fluorescence in situ hybridization: detection of a break in the centromeric alpha-satellite sequences.
Tümer Z; Berg A; Mikkelsen M
Hum Genet; 1995 Mar; 95(3):299-302. PubMed ID: 7868122
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. A de novo translocation of chromosomes 1 and 2 in an 18 year old boy with syndromic mental retardation.
Neetha J; Girisha KM; Gopinath PM; Sekhar MR
Genet Couns; 2012; 23(4):473-6. PubMed ID: 23431746
[TBL] [Abstract][Full Text] [Related]
32. De novo unbalanced translocation 2;4 characterized by metaphase CGH and array CGH in a child with mental retardation and dysmorphic features.
Debost-Legrand A; Capri Y; Gouas L; Pebrel-Richard C; Veronese L; Tchirkov A; Haoud K; Boespflug-Tanguy O; Goumy C; Vago P
Pathol Biol (Paris); 2011 Dec; 59(6):309-13. PubMed ID: 21145667
[TBL] [Abstract][Full Text] [Related]
33. Complex Rearrangement Involving Three Chromosomes, Four Breakpoints and a 2.7-Mb Deletion in the 18q Segment Observed in a Girl with Mild Learning Difficulties.
Kontodiou M; Daskalakis G; Vetro A; Paspaliaris V; Papaioannou G; Dagklis T; Tsakiridis I; Ziegler M; Liehr T; Thomaidis L; Papoulidis I; Manolakos E
Cytogenet Genome Res; 2015; 147(2-3):118-23. PubMed ID: 26681178
[TBL] [Abstract][Full Text] [Related]
34. [Case of subtelomeric aberration as a cause of familial intellectual disability with congenital defects and dysmorphic features--problems of diagnosis and genetic counseling].
Obersztyn E; Mazurczak T; Helias-Rodzewicz Z; Bocian E; Kutkowska-Kazmierczak A
Med Wieku Rozwoj; 2003; 7(3):389-401. PubMed ID: 14963346
[TBL] [Abstract][Full Text] [Related]
35. A case of 46,XY,t(1;13) (q24;q32) with mental retardation.
Wilbur L; Curcuru-Giordano FM; Krishna SG; Kardon NB; Jenkins EC
Hum Genet; 1977 Jun; 37(2):239-42. PubMed ID: 885541
[TBL] [Abstract][Full Text] [Related]
36. Gene for incontinentia pigmenti maps to band Xp11 with an (X;10) (p11;q22) translocation.
Cannizzaro LA; Hecht F
Clin Genet; 1987 Jul; 32(1):66-9. PubMed ID: 3621656
[TBL] [Abstract][Full Text] [Related]
37. Molecular characterisation of a mosaicism with a complex chromosome rearrangement: evidence for coincident chromosome healing by telomere capture and neo-telomere formation.
Chabchoub E; Rodríguez L; Galán E; Mansilla E; Martínez-Fernandez ML; Martínez-Frías ML; Fryns JP; Vermeesch JR
J Med Genet; 2007 Apr; 44(4):250-6. PubMed ID: 17172463
[TBL] [Abstract][Full Text] [Related]
38. [Genetic analysis of a patient featuring developmental delay and mental retardation].
Bai N; Liu Y; Mei S; Kong X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):208-11. PubMed ID: 27060317
[TBL] [Abstract][Full Text] [Related]
39. SOD-A and chromosome 21. Conflicting findings in a familial translocation (9p24;21q214).
Leschot NJ; Slater RM; Joenje H; Becker-Bloemkolk MJ; de Nef JJ
Hum Genet; 1981; 57(2):220-3. PubMed ID: 7228038
[TBL] [Abstract][Full Text] [Related]
40. Ring chromosome 22 in a mentally retarded child and mosaic 45,XX,-15,-22,+t(15;22)(p11;q11)/46,XX,r(22)/46,XX karyotype in the mother.
Fryns JP; Van den Berghe H
Hum Genet; 1979 Mar; 47(2):213-6. PubMed ID: 437787
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
