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Results: 1 to 20 of 104

Similar articles for PubMed (Select 23259705)

1.

Absence of subtelomeric rearrangements in selected patients with mental retardation as assessed by multiprobe T FISH.

dos Santos SR, Freire-Maia DV.

J Negat Results Biomed. 2012 Dec 21;11:16. doi: 10.1186/1477-5751-11-16.

2.

Subtelomeric chromosome rearrangements in children with idiopathic mental retardation: applicability of three molecular-cytogenetic methods.

Erjavec-Skerget A, Stangler-Herodez S, Zagorac A, Zagradisnik B, Kokalj-Vokac N.

Croat Med J. 2006 Dec;47(6):841-50.

3.
4.

[Detection of subtelomeric rearrangements in patients with idiopathic mental retardation/developmental delay].

Wu Y, Jiang YW, Wang XZ, Wang HF, Wang JM, Yang YL, Qin J, Zhong N, Wu XR.

Zhonghua Er Ke Za Zhi. 2007 Dec;45(12):906-11. Chinese.

PMID:
18339278
5.

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.

PMID:
15039644
6.

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 Oct-Dec;48(4):388-96.

PMID:
16378923
7.

Chromosomal rearrangements in children with idiopathic mental retardation using subtelomeric fluorescent in situ hybridization.

Cogulu O, Gunduz C, Karaca E, Onay H, Ozkinay C, Ozkinay F.

Genet Couns. 2006;17(3):321-31.

PMID:
17100201
8.

Subtelomeric rearrangements of dysmorphic children with idiopathic mental retardation reveal 8 different chromosomal anomalies.

Mihçi E, Ozcan M, Berker-Karaüzüm S, Keser I, Taçoy S, Hapsolat S, Lüleci G.

Turk J Pediatr. 2009 Sep-Oct;51(5):453-9.

10.

MLPA vs multiprobe FISH: comparison of two methods for the screening of subtelomeric rearrangements in 50 patients with idiopathic mental retardation.

Palomares M, Delicado A, Lapunzina P, Arjona D, Amiñoso C, Arcas J, Martinez Bermejo A, Fernández L, López Pajares I.

Clin Genet. 2006 Mar;69(3):228-33.

PMID:
16542387
11.
12.

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 15;140(2):144-50.

PMID:
16353244
13.

Utility of subtelomeric fluorescent DNA probes for detection of chromosome anomalies in 425 patients.

Jalal SM, Harwood AR, Sekhon GS, Pham Lorentz C, Ketterling RP, Babovic-Vuksanovic D, Meyer RG, Ensenauer R, Anderson MH Jr, Michels VV.

Genet Med. 2003 Jan-Feb;5(1):28-34.

PMID:
12544473
14.

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.

PMID:
16080292
15.

Subtelomeric rearrangements in idiopathic mental retardation.

Velagaleti GV, Robinson SS, Rouse BM, Tonk VS, Lockhart LH.

Indian J Pediatr. 2005 Aug;72(8):679-85.

PMID:
16131774
16.

Primed in situ labeling technique for subtelomeric rearrangements in 70 children with idiopathic mental retardation.

Tian H, Yu H, Fu S, Jin R.

J Huazhong Univ Sci Technolog Med Sci. 2011 Dec;31(6):834-6. doi: 10.1007/s11596-011-0686-7. Epub 2011 Dec 16.

PMID:
22173508
17.

Detecting rearrangements in children using subtelomeric FISH and SKY.

Clarkson B, Pavenski K, Dupuis L, Kennedy S, Meyn S, Nezarati MM, Nie G, Weksberg R, Withers S, Quercia N, Teebi AS, Teshima I.

Am J Med Genet. 2002 Feb 1;107(4):267-74.

PMID:
11840482
18.
19.

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 17;6:21.

20.

[Familial subtelomeric abnormality der(4)t(4p16.3;21q22.3) as a cause of mental retardation and mild dysmorphic features].

Obersztyn E, Klapecki J, Helias-Rodzewicz Z, Bocian E, Mazurczak T.

Med Wieku Rozwoj. 2006 Jan-Mar;10(1 Pt 2):199-209. Polish.

PMID:
17028389
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