434 related articles for article (PubMed ID: 10797432)
1. Mosaic rearrangement of chromosome 18: characterization by FISH mapping and DNA studies shows trisomy 18p and monosomy 18p both of paternal origin.
Oner G; Jauch A; Eggermann T; Hardwick R; Kirsch S; Schiebel K; Rappold G; Robson L; Smith A
Am J Med Genet; 2000 May; 92(2):101-6. PubMed ID: 10797432
[TBL] [Abstract][Full Text] [Related]
2. Clinical outcome: a monosomy 18p is better than a tetrasomy 18p.
Wei J; Xie Y; He W; Liu W; Jian W; Chen M; Wang D; Wang X; Sun X
Cytogenet Genome Res; 2014; 144(4):294-8. PubMed ID: 25634515
[TBL] [Abstract][Full Text] [Related]
3. Recurrent proximal 18p monosomy and 18q trisomy in a family with a maternal pericentric inversion of chromosome 18.
Prabhakara K; Wyandt HE; Huang XL; Prasad KS; Ramadevi AR
Ann Genet; 2004; 47(3):297-303. PubMed ID: 15337476
[TBL] [Abstract][Full Text] [Related]
4. A de novo subterminal trisomy 10p and monosomy 18q in a girl with MCA/MR: case report and review.
Courtens W; Wuyts W; Scheers S; Van Luijk R; Reyniers E; Rooms L; Ceulemans B; Kooy F; Wauters J
Eur J Med Genet; 2006; 49(5):402-13. PubMed ID: 16488200
[TBL] [Abstract][Full Text] [Related]
5. Molecular cytogenetic characterization of 18;21 whole arm translocation associated with monosomy 18p.
Wang JC; Nemana L; Kou SY; Habibian R; Hajianpour MJ
Am J Med Genet; 1997 Sep; 71(4):463-6. PubMed ID: 9286456
[TBL] [Abstract][Full Text] [Related]
6. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
Chen CP; Chern SR; Wang W; Lee CC; Chen WL; Chen LF; Chang TY; Tzen CY
Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
[TBL] [Abstract][Full Text] [Related]
7. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example.
Fryns JP; Kleczkowska A; Jaeken J; Van Herck K; Van den Berghe MH
Ann Genet; 1989; 32(3):177-9. PubMed ID: 2486064
[TBL] [Abstract][Full Text] [Related]
8. 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]
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. Prenatal diagnosis and clinical features of an individual with tetrasomy 18p and trisomy 18q mosaicism.
Habecker-Green JG; Naeem R; Gold H; O'Grady JP; Kanaan C; Bayer-Zwirello L; Murray MS; Cohn GM
J Perinatol; 1998; 18(5):395-8. PubMed ID: 9766419
[TBL] [Abstract][Full Text] [Related]
11. Presumptive monosomy 21 with neuronal migration disorder re-diagnosed as de novo unbalanced translocation t(18p;21q) by fluorescence in situ hybridisation.
Alkan M; Ramelli GP; Hirsiger H; Keser I; Remonda L; Bühler EM; Moser H
Genet Couns; 2002; 13(2):151-6. PubMed ID: 12150215
[TBL] [Abstract][Full Text] [Related]
12. An unusual case of monosomy 18p: minor malformations with speech delay.
Bora E; Giray O; Ulgenalp A; Ozkan H; Erçal D
Turk J Pediatr; 2005; 47(2):199-201. PubMed ID: 16052867
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
Chen CP; Chern SR; Wang TH; Hsueh DW; Lee CC; Town DD; Wang W; Ko TM
Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
[TBL] [Abstract][Full Text] [Related]
14. Partial 18q trisomy and 18p monosomy resulting from a maternal pericentric inversion, inv(18)(p11.2q21.3).
Asano T; Ikeuchi T; Shinohara T; Enokido H; Hashimoto K
Jinrui Idengaku Zasshi; 1991 Sep; 36(3):257-65. PubMed ID: 1753439
[TBL] [Abstract][Full Text] [Related]
15. Fluorescence in situ hybridization (FISH) of a whole-arm translocation involving chromosomes 18 and 20 with alpha-satellite DNA probes: detection of a centromeric DNA break?
Cantú ES; Khan TA; Pai GS
Am J Med Genet; 1992 Oct; 44(3):340-4. PubMed ID: 1488982
[TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18p.
McGhee EM; Qu Y; Wohlferd MM; Goldberg JD; Norton ME; Cotter PD
Clin Genet; 2001 Apr; 59(4):274-8. PubMed ID: 11298684
[TBL] [Abstract][Full Text] [Related]
17. Unusual mosaic trisomy 13 through 13/13 translocation and monosomy 13 with a small ring.
Jalal SM; Martin JA; Benjamin TR; Kukolich MK; Townsend-Parcham JK
Ann Genet; 1990; 33(3):173-5. PubMed ID: 2288463
[TBL] [Abstract][Full Text] [Related]
18. A rare case of monosomy 18p: translocation between chromosomes 18 and 21.
Tos T; Karaman A; Aycan Z; Tükün A
Genet Couns; 2011; 22(2):227-31. PubMed ID: 21848017
[TBL] [Abstract][Full Text] [Related]
19. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
Esmer MC; Carnevale A; Gómez L; del Castillo V; Frías S
Rev Invest Clin; 1996; 48(1):27-33. PubMed ID: 8815483
[TBL] [Abstract][Full Text] [Related]
20. Formation of supernumerary euchromatic short arm isochromosomes: parent and cell stage of origin in new cases and review of the literature.
Eggermann T; Schubert R; Engels H; Apacik C; Stengel-Rutkowski S; Haefliger C; Emiliani V; Ricagni C; Schwanitz G
Ann Genet; 1999; 42(2):75-80. PubMed ID: 10434120
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]