214 related articles for article (PubMed ID: 10751083)
1. Duplication of chromosome region 8p23.1-->p23.3: a benign variant?
Engelen JJ; Moog U; Evers JL; Dassen H; Albrechts JC; Hamers AJ
Am J Med Genet; 2000 Mar; 91(1):18-21. PubMed ID: 10751083
[TBL] [Abstract][Full Text] [Related]
2. Duplication of 8p23.2: a benign cytogenetic variant?
Harada N; Takano J; Kondoh T; Ohashi H; Hasegawa T; Sugawara H; Ida T; Yoshiura K; Ohta T; Kishino T; Kajii T; Niikawa N; Matsumoto N
Am J Med Genet; 2002 Aug; 111(3):285-8. PubMed ID: 12210324
[TBL] [Abstract][Full Text] [Related]
3. Report of a patient with a trisomy of chromosome region 20q11.2-->20q12 and characterization with FISH.
Wanderley HY; Schrander-Stumpel CT; Visser MO; Van Maanen-Op Het Roodt EA; Loneus WH; Engelen JJ
Genet Couns; 2005; 16(3):277-82. PubMed ID: 16259325
[TBL] [Abstract][Full Text] [Related]
4. Duplication within chromosome region 15q11-q13 in a patient with similarities to Prader-Willi syndrome confirmed by region-specific and band-specific fish.
Engelen JJ; Loots WJ; Albrechts JC; Schrander-Stumpel CT; Dirckx R; Smeets HJ; Hamers AJ; Geraedts JP
Genet Couns; 1999; 10(2):123-32. PubMed ID: 10422004
[TBL] [Abstract][Full Text] [Related]
5. Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level.
Barber JC; Maloney V; Hollox EJ; Stuke-Sontheimer A; du Bois G; Daumiller E; Klein-Vogler U; Dufke A; Armour JA; Liehr T
Eur J Hum Genet; 2005 Oct; 13(10):1131-6. PubMed ID: 16077733
[TBL] [Abstract][Full Text] [Related]
6. Delimitation of duplicated segments and identification of their parental origin in two partial chromosome 3p duplications.
Antonini S; Kim CA; Sugayama SM; Vianna-Morgante AM
Am J Med Genet; 2002 Nov; 113(2):144-50. PubMed ID: 12407704
[TBL] [Abstract][Full Text] [Related]
7. Duplication of 9 p11.2-p13.1: a benign cytogenetic variant.
Di Giacomo MC; Cesarano C; Bukvic N; Manisali E; Guanti G; Susca F
Prenat Diagn; 2004 Aug; 24(8):619-22. PubMed ID: 15305349
[TBL] [Abstract][Full Text] [Related]
8. Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance.
Barber JC; Joyce CA; Collinson MN; Nicholson JC; Willatt LR; Dyson HM; Bateman MS; Green AJ; Yates JR; Dennis NR
J Med Genet; 1998 Jun; 35(6):491-6. PubMed ID: 9643291
[TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis of a half-cryptic translocation using chromosome microdissection.
Senger G; Chudoba I; Friedrich U; Tommerup N; Claussen U; Brøndum-Nielsen K
Prenat Diagn; 1997 Apr; 17(4):369-74. PubMed ID: 9160390
[TBL] [Abstract][Full Text] [Related]
10. Diagnosis of four chromosome abnormalities of unknown origin by chromosome microdissection and subsequent reverse and forward painting.
Coêlho KE; Egashira M; Kato R; Fujimoto M; Matsumoto N; Rerkamnuaychoke B; Abe K; Harada N; Ohashi H; Fukushima Y; Niikawa N
Am J Med Genet; 1996 Jun; 63(3):468-71. PubMed ID: 8737654
[TBL] [Abstract][Full Text] [Related]
11. Directly inherited partial trisomy of chromosome 6p identified in a father and daughter by chromosome microdissection.
Delatycki MB; Voullaire L; Francis D; Petrovic V; Robertson A; Webber LM; Slater HR
J Med Genet; 1999 Apr; 36(4):335-8. PubMed ID: 10227406
[TBL] [Abstract][Full Text] [Related]
12. Duplication of 11p14.3-p15.1 in a mentally retarded proband and his mother detected by G-banding and confirmed by high-resolution CGH and BAC FISH.
Wyandt HE; Shim SH; Mark HF; Huang XL; Milunsky JM
Exp Mol Pathol; 2006 Jun; 80(3):262-6. PubMed ID: 16516886
[TBL] [Abstract][Full Text] [Related]
13. Inverted duplication of chromosome 5p14p15.3 confirmed with in situ hybridization.
Zenger-Hain JL; Van Dyke DL; Wiktor A; Walker H; Feldman GL
Am J Med Genet; 1993 Dec; 47(8):1198-201. PubMed ID: 8291556
[TBL] [Abstract][Full Text] [Related]
14. Duplication of chromosome region (16)(p11.2 --> p12.1) in a mother and daughter with mild mental retardation.
Engelen JJ; de Die-Smulders CE; Dirckx R; Verhoeven WM; Tuinier S; Curfs LM; Hamers AJ
Am J Med Genet; 2002 Apr; 109(2):149-53. PubMed ID: 11977164
[TBL] [Abstract][Full Text] [Related]
15. 8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGH.
Barber JC; Maloney VK; Huang S; Bunyan DJ; Cresswell L; Kinning E; Benson A; Cheetham T; Wyllie J; Lynch SA; Zwolinski S; Prescott L; Crow Y; Morgan R; Hobson E
Eur J Hum Genet; 2008 Jan; 16(1):18-27. PubMed ID: 17940555
[TBL] [Abstract][Full Text] [Related]
16. [Analysis of complex chromosomal aberrations in patients with myelodysplastic syndromes using multiplex fluorescence in situ hybridization combined with whole chromosome painting].
Chen LJ; Li JY; Xiao B; Zhu Y; Liu Q; Pan JL; Qiu HR; Fan L; Zhang SJ; Lu RN; Xu W; Xue YQ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec; 24(6):635-9. PubMed ID: 18067073
[TBL] [Abstract][Full Text] [Related]
17. Dicentric chromosome 9 due to tandem duplication of the 9p11-q13 region: unusual chromosome 9 variant.
Lukusa T; Devriendt K; Holvoet M; Fryns JP
Am J Med Genet; 2000 Mar; 91(3):192-7. PubMed ID: 10756341
[TBL] [Abstract][Full Text] [Related]
18. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
Zhang L; Parkhurst JB; Kern WF; Scott KV; Niccum D; Mulvihill JJ; Li S
Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352
[TBL] [Abstract][Full Text] [Related]
19. Identification of autosomal supernumerary chromosome markers (SMCs) by fluorescent in situ hybridization (FISH).
Kolialexi A; Kitsiou S; Fryssira H; Sofocleous C; Kouvidi E; Tsangaris GT; Salavoura K; Mavrou A
In Vivo; 2006; 20(4):473-8. PubMed ID: 16900777
[TBL] [Abstract][Full Text] [Related]
20. Generation of FISH probes using laser microbeam microdissection and application to clinical molecular cytogenetics.
Shim SH; Kyhm JH; Chung SR; Kim SR; Park MI; Lee CH; Cho YH
J Microbiol Biotechnol; 2007 Jul; 17(7):1079-82. PubMed ID: 18051316
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
