348 related articles for article (PubMed ID: 16688748)
1. Array-based comparative genomic hybridization facilitates identification of breakpoints of a novel der(1)t(1;18)(p36.3;q23)dn in a child presenting with mental retardation.
Lennon PA; Cooper ML; Curtis MA; Lim C; Ou Z; Patel A; Cheung SW; Bacino CA
Am J Med Genet A; 2006 Jun; 140(11):1156-63. PubMed ID: 16688748
[TBL] [Abstract][Full Text] [Related]
2. Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements.
Ballif BC; Wakui K; Gajecka M; Shaffer LG
Hum Genet; 2004 Jan; 114(2):198-206. PubMed ID: 14579147
[TBL] [Abstract][Full Text] [Related]
3. Characterization of the recurrent translocation t(1;1)(p36.3;q21.1-2) in non-Hodgkin lymphoma by multicolor banding and fluorescence in situ hybridization analysis.
Lestou VS; Ludkovski O; Connors JM; Gascoyne RD; Lam WL; Horsman DE
Genes Chromosomes Cancer; 2003 Apr; 36(4):375-81. PubMed ID: 12619161
[TBL] [Abstract][Full Text] [Related]
4. Clinical and molecular cytogenetic characterization of four patients with unbalanced translocation der(1)t(1;22)(p36;q13).
Gajecka M; Saadeh R; Mackay KL; Glotzbach CD; Spodar K; Chitayat D; Shaffer LG
Am J Med Genet A; 2008 Nov; 146A(21):2777-84. PubMed ID: 18958851
[TBL] [Abstract][Full Text] [Related]
5. Monosomy 1p36 breakpoint junctions suggest pre-meiotic breakage-fusion-bridge cycles are involved in generating terminal deletions.
Ballif BC; Yu W; Shaw CA; Kashork CD; Shaffer LG
Hum Mol Genet; 2003 Sep; 12(17):2153-65. PubMed ID: 12915474
[TBL] [Abstract][Full Text] [Related]
6. Cryptic unbalanced translocation t(17;18)(p13.2;q22.3) identified by subtelomeric FISH and defined by array-based comparative genomic hybridization in a patient with mental retardation and dysmorphic features.
Hwang KS; Pearson MA; Stankiewicz P; Lennon PA; Cooper ML; Wu J; Ou Z; Cai WW; Patel A; Cheung SW
Am J Med Genet A; 2005 Aug; 137(1):88-93. PubMed ID: 16015583
[TBL] [Abstract][Full Text] [Related]
7. Breakpoint mapping in a case of mosaicism with partial monosomy 9p23 --> pter and partial trisomy 1q41 --> qter suggests neo-telomere formation in stabilizing the deleted chromosome.
Kulikowski LD; Christ LA; Nogueira SI; Brunoni D; Schwartz S; Melaragno MI
Am J Med Genet A; 2006 Jan; 140(1):82-7. PubMed ID: 16333825
[TBL] [Abstract][Full Text] [Related]
8. Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection.
Chen Z; Grebe TA; Guan XY; Notohamiprodjo M; Nutting PJ; Stone JF; Trent JM; Sandberg AA
Am J Med Genet; 1997 Aug; 71(2):160-6. PubMed ID: 9217215
[TBL] [Abstract][Full Text] [Related]
9. Girl with monosomy 1p36 and Angelman syndrome due to unbalanced der(1) transmission of a maternal translocation t(1;15)(p36.3;q13.1).
Torisu H; Yamamoto T; Fujiwaki T; Kadota M; Oshimura M; Kurosawa K; Akaboshi S; Oka A
Am J Med Genet A; 2004 Nov; 131(1):94-8. PubMed ID: 15384094
[TBL] [Abstract][Full Text] [Related]
10. Trisomy of 8q22.3 approximately q23-qter following an unbalanced 1;8 translocation in a boy with multiple anomalies.
Ergun MA; Balci S; Konaç E; Kan D; Menevşe S; Bartsch O
Turk J Pediatr; 2004; 46(4):384-7. PubMed ID: 15641279
[TBL] [Abstract][Full Text] [Related]
11. Mild craniosynostosis with 1p36.3 trisomy and 1p36.3 deletion syndrome caused by familial translocation t(Y;1).
Hiraki Y; Fujita H; Yamamori S; Ohashi H; Eguchi M; Harada N; Mizuguchi T; Matsumoto N
Am J Med Genet A; 2006 Aug; 140(16):1773-7. PubMed ID: 16835918
[TBL] [Abstract][Full Text] [Related]
12. Identification of the breakpoints at 1p36.2 and 3p21.3 in an AML(M3) patient who had t(1;3)(p36.2;p21.3) at the third relapse.
Tri NK; Xinh PT; Nagao H; Izumi T; Ozawa K; Toyoda A; Hattori M; Sakaki Y; Tokunaga K; Sato Y
Genes Chromosomes Cancer; 2002 Dec; 35(4):365-7. PubMed ID: 12378531
[TBL] [Abstract][Full Text] [Related]
13. Molecular characterization of a patient with central nervous system dysmyelination and cryptic unbalanced translocation between chromosomes 4q and 18q.
Gunn SR; Mohammed M; Reveles XT; Viskochil DH; Palumbos JC; Johnson-Pais TL; Hale DE; Lancaster JL; Hardies LJ; Boespflug-Tanguy O; Cody JD; Leach RJ
Am J Med Genet A; 2003 Jul; 120A(1):127-35. PubMed ID: 12794705
[TBL] [Abstract][Full Text] [Related]
14. Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.
Chen CP; Chen M; Su YN; Hsu CY; Tsai FJ; Chern SR; Wu PC; Lee CC; Wang W
Taiwan J Obstet Gynecol; 2010 Dec; 49(4):473-80. PubMed ID: 21199750
[TBL] [Abstract][Full Text] [Related]
15. Detection of cryptic chromosome aberrations in a patient with a balanced t(1;9)(p34.2;p24) by array-based comparative genomic hybridization.
Hayashi S; Kurosawa K; Imoto I; Mizutani S; Inazawa J
Am J Med Genet A; 2005 Nov; 139(1):32-6. PubMed ID: 16222686
[TBL] [Abstract][Full Text] [Related]
16. Cytogenetic and array CGH characterization of de novo 1p36 duplications and deletion in a patient with congenital cataracts, hearing loss, choanal atresia, and mental retardation.
Chen E; Obolensky E; Rauen KA; Shaffer LG; Li X
Am J Med Genet A; 2008 Nov; 146A(21):2785-90. PubMed ID: 18924166
[TBL] [Abstract][Full Text] [Related]
17. Identification of a 650 kb duplication at the X chromosome breakpoint in a patient with 46,X,t(X;8)(q28;q12) and non-syndromic mental retardation.
Cox JJ; Holden ST; Dee S; Burbridge JI; Raymond FL
J Med Genet; 2003 Mar; 40(3):169-74. PubMed ID: 12624134
[TBL] [Abstract][Full Text] [Related]
18. Rearrangements of chromosome band 1p36 in non-Hodgkin's lymphoma.
Dave BJ; Hess MM; Pickering DL; Zaleski DH; Pfeifer AL; Weisenburger DD; Armitage JO; Sanger WG
Clin Cancer Res; 1999 Jun; 5(6):1401-9. PubMed ID: 10389925
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Familial MCA/MR syndrome due to inherited submicroscopic translocation t(18;21)(q22.1q21.3) with breakpoint at the Down syndrome critical region.
Horn D; Neitzel H; Tönnies H; Kalscheuer V; Kunze J; Hinkel GK; Bartsch O
Am J Med Genet A; 2003 Mar; 117A(3):236-44. PubMed ID: 12599186
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
