229 related articles for article (PubMed ID: 10227406)
1. 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]
2. Duplication 20p identified via fluorescent in situ hybridization.
LeChien KA; McPherson E; Estop AM
Am J Med Genet; 1994 Apr; 50(2):187-9. PubMed ID: 7516625
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome.
Ausems MG; Schuil J; Van Raveswaaij-Arts C; De Pater JM
Genet Couns; 2004; 15(4):405-10. PubMed ID: 15658615
[TBL] [Abstract][Full Text] [Related]
5. Paternal origin of der(X)t(X;6) in a girl with trisomy 6p and unbalanced t(6;10) mosaicism in her mother.
Petković I; Barisić I; Bastić M; Hećimović S; Bago R
Am J Med Genet A; 2003 Jul; 120A(2):266-71. PubMed ID: 12833412
[TBL] [Abstract][Full Text] [Related]
6. [Clinical and molecular cytogenetic analysis of a rare case of mosaicism for partial monosomy 3p and partial trisomy 10q in human].
Karamysheva TV; Matveeva VG; Shorina AP; Rubtsov NB
Genetika; 2001 Jun; 37(6):811-6. PubMed ID: 11517768
[TBL] [Abstract][Full Text] [Related]
7. Joubert syndrome co-existing with partial Xp trisomy: review of the literature.
Güven GS; Fenerci EY; Deviren A; Ozkiliç A; Yüksel A; Hacihanefioğlu S
Genet Couns; 2004; 15(3):321-8. PubMed ID: 15517825
[TBL] [Abstract][Full Text] [Related]
8. [Cytogenetic and molecular characterization of partial trisomy 4q and partial monosomy 10q in a patient].
Zhang YL; Dai Y; Tu ZG; Li QY; Wang LQ; Zhang L; Zeng J; Ouyang ZB
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Apr; 27(2):153-7. PubMed ID: 20376795
[TBL] [Abstract][Full Text] [Related]
9. Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblings.
Hegmann KM; Spikes AS; Orr-Urtreger A; Shaffer LG
Am J Med Genet; 1996 Jan; 61(1):10-5. PubMed ID: 8741910
[TBL] [Abstract][Full Text] [Related]
10. Familial translocation t(6;20)(p21;p13) resulting in partial trisomy 6p and partial monosomy 20p: report of a new case and review of the literature.
Berner AL; Bağci S; Wohlleber E; Engels E; Müller A; Bartmann P; Weber RG; Reutter H
Cytogenet Genome Res; 2012; 136(4):308-13. PubMed ID: 22433391
[TBL] [Abstract][Full Text] [Related]
11. Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome.
Lukusa T; van den Berghe L; Smeets E; Fryns JP
Ann Genet; 1999; 42(4):215-20. PubMed ID: 10674161
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Distal monosomy 16p13.3/distal trisomy 2p24.2-pter: molecular-cytogenetic characterisation and phenotype.
Mach M; Windpassinger C; Wagner K; Kroisel PM; Petek E
Genet Couns; 2007; 18(1):9-16. PubMed ID: 17515297
[TBL] [Abstract][Full Text] [Related]
15. Duplication 5q and deletion 9p due to a t(5;9)(q34;p23) in 2 cousins with features of Hunter-McAlpine syndrome and hypothyroidism.
Vásquez-Velásquez AI; García-Castillo HA; González-Mercado MG; Dávalos IP; Raca G; Xu X; Dwyer E; Rivera H
Cytogenet Genome Res; 2011; 132(4):233-8. PubMed ID: 21063078
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Huang JK; Lee CC; Wang W
Genet Couns; 2006; 17(1):57-63. PubMed ID: 16719278
[TBL] [Abstract][Full Text] [Related]
18. A familial complex chromosome translocation resulting in duplication of 6p25.
Vermeesch JR; Thoelen R; Fryns JP
Ann Genet; 2004; 47(3):275-80. PubMed ID: 15337473
[TBL] [Abstract][Full Text] [Related]
19. Trisomy 2q35-q37 due to insertion of 2q material into 17q25: clinical, cytogenetic, and molecular cytogenetic characterization.
Fritz B; Müller-Navia J; Hillig U; Köhler M; Aslan M; Rehder H
Am J Med Genet; 1999 Dec; 87(4):297-301. PubMed ID: 10588833
[TBL] [Abstract][Full Text] [Related]
20. Identification and molecular confirmation of a small chromosome 10q duplication [dir dup(10)(q24.2-->q24.3)] inherited from a mother mosaic for the abnormality.
Tonk V; Schneider NR; Delgado MR; Mao J; Schultz RA
Am J Med Genet; 1996 Jan; 61(1):16-20. PubMed ID: 8741911
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]