228 related articles for article (PubMed ID: 12808681)
1. Multiple fetal anomalies associated with subtle subtelomeric chromosomal rearrangements.
Souter VL; Glass IA; Chapman DB; Raff ML; Parisi MA; Opheim KE; Disteche CM
Ultrasound Obstet Gynecol; 2003 Jun; 21(6):609-15. PubMed ID: 12808681
[TBL] [Abstract][Full Text] [Related]
2. Subtelomeric chromosomal rearrangements detected in patients with idiopathic mental retardation and dysmorphic features.
Caliskan MO; Karauzum SB; Mihci E; Tacoy S; Luleci G
Genet Couns; 2005; 16(2):129-38. PubMed ID: 16080292
[TBL] [Abstract][Full Text] [Related]
3. Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay, M-TEL.
Brown J; Horsley SW; Jung C; Saracoglu K; Janssen B; Brough M; Daschner M; Beedgen B; Kerkhoffs G; Eils R; Harris PC; Jauch A; Kearney L
Eur J Hum Genet; 2000 Dec; 8(12):903-10. PubMed ID: 11175277
[TBL] [Abstract][Full Text] [Related]
4. Unbalanced cryptic 5p deletion/17p duplication identified by subtelomeric FISH in a family with a boy with chimerism and a balanced t(4;5).
Ensenauer R; Jalal S; Meyer R; Babovic-Vuksanovic D
Am J Med Genet A; 2004 Feb; 125A(1):86-91. PubMed ID: 14755472
[TBL] [Abstract][Full Text] [Related]
5. Unbalanced translocation 6p/16q (partial monosomy 6p and trisomy 16q): prenatal diagnosis and cytogenetics.
Puhl AG; Zelazny J; Galetzka D; Skala C; Frey-Mahn G; Wellek B; Koelbl H
Eur J Obstet Gynecol Reprod Biol; 2010 Jun; 150(2):119-25. PubMed ID: 20211513
[TBL] [Abstract][Full Text] [Related]
6. Complex de novo cryptic subtelomeric rearrangements in a fetus with multiple ultrasonographic abnormalities and a normal karyotype at amniocentesis.
Iqbal MA; Ramadan S; Ali FA; Kurdi W
Prenat Diagn; 2005 Dec; 25(12):1142-9. PubMed ID: 16240463
[TBL] [Abstract][Full Text] [Related]
7. Cryptic subtelomeric translocations in the 22q13 deletion syndrome.
Praphanphoj V; Goodman BK; Thomas GH; Raymond GV
J Med Genet; 2000 Jan; 37(1):58-61. PubMed ID: 10633138
[TBL] [Abstract][Full Text] [Related]
8. Unexpected retention and concomitant loss of subtelomeric regions in balanced chromosome anomalies by FISH.
Pettenati MJ; Jackle B; Bobby P; Stewart W; Von Kap-Herr C; Mowrey P; Rao PN; May KM
Am J Med Genet; 2002 Jul; 111(1):48-53. PubMed ID: 12124733
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Prenatal diagnosis of de novo unbalanced translocation 8p;21q using subtelomeric probes.
Ozkinay F; Kanit H; Onay H; Cogulu O; Gunduz C; Ercal D; Ozkinay C
Genet Couns; 2006; 17(3):315-20. PubMed ID: 17100200
[TBL] [Abstract][Full Text] [Related]
11. Prenatal detection of a subtle unbalanced chromosome rearrangement by karyotyping, FISH and array comparative genomic hybridization.
Cain CC; Saul DO; Oehler E; Blakemore K; Stetten G
Fetal Diagn Ther; 2008; 24(3):286-90. PubMed ID: 18818501
[TBL] [Abstract][Full Text] [Related]
12. Familial cryptic (20;21) translocation identified by in situ hybridization technologies.
Leppig KA; Ball S; Au K; Opheim KE; Norwood T
Am J Med Genet; 2000 Aug; 93(4):273-7. PubMed ID: 10946352
[TBL] [Abstract][Full Text] [Related]
13. Fetal karyotyping after 28 weeks of gestation for late ultrasound findings in a low risk population.
Drummond CL; Gomes DM; Senat MV; Audibert F; Dorion A; Ville Y
Prenat Diagn; 2003 Dec; 23(13):1068-72. PubMed ID: 14691994
[TBL] [Abstract][Full Text] [Related]
14. A case of recurrent congenital fetal anomalies associated with a familial subtelomeric translocation.
Brackley KJ; Kilby MD; Morton J; Whittle MJ; Knight SJ; Flint J
Prenat Diagn; 1999 Jun; 19(6):570-4. PubMed ID: 10416976
[TBL] [Abstract][Full Text] [Related]
15. Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qter.
Sogaard M; Tümer Z; Hjalgrim H; Hahnemann J; Friis B; Ledaal P; Pedersen VF; Baekgaard P; Tommerup N; Cingöz S; Duno M; Brondum-Nielsen K
BMC Med Genet; 2005 May; 6():21. PubMed ID: 15904506
[TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
Chen CP; Chern SR; Lee CC; Lin CC; Li YC; Hsieh LJ; Chen WL; Wang W
Prenat Diagn; 2006 Feb; 26(2):138-46. PubMed ID: 16470734
[TBL] [Abstract][Full Text] [Related]
17. Familial complex 3q;10q rearrangement unraveled by subtelomeric FISH analysis.
Battaglia A; Novelli A; Ceccarini C; Carey JC
Am J Med Genet A; 2006 Jan; 140(2):144-50. PubMed ID: 16353244
[TBL] [Abstract][Full Text] [Related]
18. Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype.
Chen M; Hwu WL; Kuo SJ; Chen CP; Yin PL; Chang SP; Lee DJ; Chen TH; Wang BT; Lin CC
Ultrasound Obstet Gynecol; 2006 Dec; 28(7):939-43. PubMed ID: 17121426
[TBL] [Abstract][Full Text] [Related]
19. Detection of cryptic subtelomeric imbalances in fetuses with ultrasound abnormalities.
Faas BH; Nillesen W; Vermeer S; Weghuis DO; de Leeuw N; Smits AP; van Ravenswaaij-Arts CM
Eur J Med Genet; 2008; 51(6):511-9. PubMed ID: 18691679
[TBL] [Abstract][Full Text] [Related]
20. Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibs.
Wieczorek D; Engels H; Viersbach R; Henke B; Schwanitz G; Passarge E
J Med Genet; 1998 Jul; 35(7):545-53. PubMed ID: 9678698
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
