138 related articles for article (PubMed ID: 21204237)
1. Trisomy 18 caused by isochromosome 18p and 18q formation: Is there a milder phenotype?
Maruotti GM; Fabbrini F; Napolitano R; Genesio R; Conti A; Mallia Milanes G; Mazzarelli LL; Martinelli P
Am J Med Genet A; 2011 Jan; 155A(1):225-7. PubMed ID: 21204237
[No Abstract] [Full Text] [Related]
2. Prenatal detection of trisomy 18 caused by isochromosome 18p and 18q formation.
van den Berg C; Pijpers L; Halley DJ; Opstal DV; Los FJ
Am J Med Genet; 1999 Sep; 86(2):151-5. PubMed ID: 10449651
[TBL] [Abstract][Full Text] [Related]
3. Suspected gonadal mosaicism for isochromosomes 18p and 18q unsubstantiated by fluorescence in situ hybridization analysis of sperm.
Williams MS; Josephson KD; Gursoy N; Jackson-Cook C
Genet Med; 2001; 3(4):318-20. PubMed ID: 11478534
[TBL] [Abstract][Full Text] [Related]
4. Different conformation of two supernumerary 18p isochromosomes, one with a concomitant partial 18q trisomy.
Noronha Dutra AR; Mancini TI; Satomi Takeno S; Moysés Oliveira M; Kim CA; Alvarez Perez AB; Domenici Kulikowski L; Melaragno MI
Cytogenet Genome Res; 2012; 138(1):1-4. PubMed ID: 22796746
[TBL] [Abstract][Full Text] [Related]
5. Trisomy 18p caused by a supernumerary marker with a chromosome 13/21 centromere: a possible recurrent chromosome aberration.
Plaja A; Lloveras E; Martinez-Bouzas C; Barreña B; Del Campo M; Fernández A; Herrero M; Barranco L; Palau N; López-Aríztegui MA; Català V; Tejada MI
Am J Med Genet A; 2013 Sep; 161A(9):2363-8. PubMed ID: 23894094
[TBL] [Abstract][Full Text] [Related]
6. Pure trisomy 20p resulting from isochromosome formation and whole arm translocation.
Sidwell RU; Pinson MP; Gibbons B; Byatt SA; Svennevik EC; Hastings RJ; Flynn DM
J Med Genet; 2000 Jun; 37(6):454-8. PubMed ID: 10928855
[No Abstract] [Full Text] [Related]
7. Prenatal detection of structural abnormalities of chromosome 18: associations with interphase fluorescence in situ hybridization (FISH) and maternal serum screening.
Graf MD; Gill P; Krew M; Schwartz S
Prenat Diagn; 2002 Aug; 22(8):645-8. PubMed ID: 12210569
[TBL] [Abstract][Full Text] [Related]
8. Prenatal detection of short arm deletion and isochromosome 18 formation investigated by molecular techniques.
Qumsiyeh MB; Tomasi A; Taslimi M
J Med Genet; 1995 Dec; 32(12):991-3. PubMed ID: 8825933
[TBL] [Abstract][Full Text] [Related]
9. Two-Generation Transmission of Trisomy 18p: Prenatal Diagnosis in a Woman with Mild Intellectual Disability.
Yu Y; Jiang Y; Hu X; Zhang H; Liu R; Wang R
Cytogenet Genome Res; 2019; 157(4):220-226. PubMed ID: 30939474
[TBL] [Abstract][Full Text] [Related]
10. Partial trisomy 18q11.2-->qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization.
Semerci CN; Bahce M; Atik F; Candemir Z; Kiraz IK; Zorlu P; Gül D
Ann Genet; 2004; 47(4):393-8. PubMed ID: 15581838
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Tetrasomy 18p caused by paternal meiotic nondisjunction.
Eggermann T; Engels H; Apacik C; Moskalonek B; Müller-Navia J; Schwanitz G; Stengel-Rutkowski S
Eur J Hum Genet; 1997; 5(3):175-7. PubMed ID: 9272743
[No Abstract] [Full Text] [Related]
13. A patient with isochromosome 18q, radial-thumb aplasia, thrombocytopenia, and an unbalanced 10;18 chromosome translocation.
Sahoo T; Naeem R; Pham K; Chheng S; Noblin ST; Bacino CA; Gambello MJ
Am J Med Genet A; 2005 Feb; 133A(1):93-8. PubMed ID: 15637724
[TBL] [Abstract][Full Text] [Related]
14. Identification of complex chromosome 18 rearrangements by FISH and array CGH in two patients with apparent isochromosome 18q.
Breman AM; Probst FJ; Blazo MA; Schaaf CP; Roney EK; Craigen WJ; Bacino CA; Cheung SW
Am J Med Genet A; 2011 Jun; 155A(6):1465-8. PubMed ID: 21567909
[No Abstract] [Full Text] [Related]
15. Prenatal diagnosis of 18p deletion and isochromosome 18q mosaicism in a fetus with a cystic hygroma.
Vičić A; Hafner T; Wagner J; Stipoljev F
Coll Antropol; 2014 Sep; 38(3):1059-62. PubMed ID: 25420396
[TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis of tetrasomy 18p using multiplex fluorescent PCR and comparison with a variety of techniques.
Irwin DL; Bryan JL; Chan FY; Matthews PL; Healey SC; Peters M; Findlay I
Genet Test; 2003; 7(1):1-6. PubMed ID: 12820695
[TBL] [Abstract][Full Text] [Related]
17. Characterization of a Wilms tumor in a 9-year-old girl with trisomy 18.
Anderson CE; Punnett HH; Huff V; de Chadarévian JP
Am J Med Genet A; 2003 Aug; 121A(1):52-5. PubMed ID: 12900902
[TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly.
Chen CP; Kuo YK; Su YN; Chern SR; Tsai FJ; Wu PC; Chen YT; Town DD; Wang W
Taiwan J Obstet Gynecol; 2011 Jun; 50(2):182-7. PubMed ID: 21791305
[TBL] [Abstract][Full Text] [Related]
19. Isochromosome 18q in a girl with holoprosencephaly, DiGeorge anomaly, and streak ovaries.
van Essen AJ; Schoots CJ; van Lingen RA; Mourits MJ; Tuerlings JH; Leegte B
Am J Med Genet; 1993 Aug; 47(1):85-8. PubMed ID: 8368259
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
