256 related articles for article (PubMed ID: 12124733)
1. 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]
2. Subtelomeric rearrangements: results from FISH studies in 84 families with idiopathic mental retardation.
Bocian E; Hélias-Rodzewicz Z; Suchenek K; Obersztyn E; Kutkowska-Kaźmierczak A; Stankiewicz P; Kostyk E; Mazurczak T
Med Sci Monit; 2004 Apr; 10(4):CR143-51. PubMed ID: 15039644
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Cryptic 6q subtelomeric deletion associated with a paracentric inversion in a mildly retarded child.
Lorda-Sanchez I; Lopez-Pajares I; Roche MC; Sanz R; Rodriguez de Alba M; Gonzalez-Gonzalez MC; Ibañez A; Ramos C; Ayuso C
Am J Med Genet; 2000 Dec; 95(4):336-8. PubMed ID: 11186887
[TBL] [Abstract][Full Text] [Related]
5. Subtelomeric rearrangements: results from a study of selected and unselected probands with idiopathic mental retardation and control individuals by using high-resolution G-banding and FISH.
Joyce CA; Dennis NR; Cooper S; Browne CE
Hum Genet; 2001 Oct; 109(4):440-51. PubMed ID: 11702226
[TBL] [Abstract][Full Text] [Related]
6. Subtelomeric chromosome aberrations: still a lot to learn.
Moog U; Arens YH; van Lent-Albrechts JC; Huijts PE; Smeets EE; Schrander-Stumpel CT; Engelen JJ
Clin Genet; 2005 Nov; 68(5):397-407. PubMed ID: 16207207
[TBL] [Abstract][Full Text] [Related]
7. Frequency of chromosome healing and interstitial telomeres in 40 cases of constitutional abnormalities.
Fortin F; Beaulieu Bergeron M; Fetni R; Lemieux N
Cytogenet Genome Res; 2009; 125(3):176-85. PubMed ID: 19738378
[TBL] [Abstract][Full Text] [Related]
8. Screening for subtelomeric chromosome abnormalities in children with idiopathic mental retardation using multiprobe telomeric FISH and the new MAPH telomeric assay.
Sismani C; Armour JA; Flint J; Girgalli C; Regan R; Patsalis PC
Eur J Hum Genet; 2001 Jul; 9(7):527-32. PubMed ID: 11464244
[TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.
Chen CP; Devriendt K; Chern SR; Lee CC; Wang W; Lin SP
Prenat Diagn; 2000 May; 20(5):384-9. PubMed ID: 10820405
[TBL] [Abstract][Full Text] [Related]
10. FISHing for mechanisms of cytogenetically defined terminal deletions using chromosome-specific subtelomeric probes.
Ballif BC; Kashork CD; Shaffer LG
Eur J Hum Genet; 2000 Oct; 8(10):764-70. PubMed ID: 11039576
[TBL] [Abstract][Full Text] [Related]
11. FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotype.
Baroncini A; Rivieri F; Capucci A; Croci G; Franchi F; Sensi A; Battaglia P; Aiello V; Calzolari E
Eur J Med Genet; 2005; 48(4):388-96. PubMed ID: 16378923
[TBL] [Abstract][Full Text] [Related]
12. An 11p;17p telomeric translocation in two families associated with recurrent miscarriages and Miller-Dieker syndrome.
Joyce CA; Dennis NR; Howard F; Davis LM; Thomas NS
Eur J Hum Genet; 2002 Nov; 10(11):707-14. PubMed ID: 12404102
[TBL] [Abstract][Full Text] [Related]
13. Detection of a cryptic translocation in a family with mental retardation using FISH and telomere region-specific probes.
Bacino CA; Kashork CD; Davino NA; Shaffer LG
Am J Med Genet; 2000 Jun; 92(4):250-5. PubMed ID: 10842290
[TBL] [Abstract][Full Text] [Related]
14. Comprehensive analysis of human subtelomeres with combined binary ratio labelling fluorescence in situ hybridisation.
Engels H; Ehrbrecht A; Zahn S; Bosse K; Vrolijk H; White S; Kalscheuer V; Hoovers JM; Schwanitz G; Propping P; Tanke HJ; Wiegant J; Raap AK
Eur J Hum Genet; 2003 Sep; 11(9):643-51. PubMed ID: 12939649
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. Subtelomeric FISH uncovers trisomy 14q32: lessons for imprinted regions, cryptic rearrangements and variant acrocentric short arms.
Sutton VR; Coveler KJ; Lalani SR; Kashork CD; Shaffer LG
Am J Med Genet; 2002 Sep; 112(1):23-7. PubMed ID: 12239715
[TBL] [Abstract][Full Text] [Related]
17. Clinical applications of two-color telomeric fluorescence in situ hybridization for prenatal diagnosis: identification of chromosomal translocation in five families with recurrent miscarriages or a child with multiple congenital anomalies.
Wakui K; Tanemura M; Suzumori K; Hidaka E; Ishikawa M; Kubota T; Fukushima Y
J Hum Genet; 1999; 44(2):85-90. PubMed ID: 10083730
[TBL] [Abstract][Full Text] [Related]
18. Detection of cryptic subtelomeric chromosome abnormalities and identification of anonymous chromatin using a quantitative multiplex ligation-dependent probe amplification (MLPA) assay.
Northrop EL; Ren H; Bruno DL; McGhie JD; Coffa J; Schouten J; Choo KH; Slater HR
Hum Mutat; 2005 Nov; 26(5):477-86. PubMed ID: 16170807
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Balanced complex chromosomal rearrangements (BCCR) with at least three chromosomes and three or more breakpoints: report of three new cases.
Lespinasse J; Réthoré MO; North MO; Bovier-Lapierre M; Lundsteen C; Fert-Ferrer S; Bugge M; Kirchoff M
Ann Genet; 2004; 47(3):315-24. PubMed ID: 15337478
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
