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Results: 1 to 20 of 410

1.

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.

PMID:
16240463
[PubMed - indexed for MEDLINE]
2.
3.

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.

PMID:
12808681
[PubMed - indexed for MEDLINE]
Free Article
4.

[Prenatal diagnosis of de novo complex balanced rearrangements in chromosomes 3,4, and 13] ].

Balícek P, Jüttnerová V, Jarosová M, Fialová J, Fiedler Z, Kolmanová J.

Cas Lek Cesk. 2001 Mar 1;140(4):122-4. Czech.

PMID:
11284430
[PubMed - indexed for MEDLINE]
5.

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.

PMID:
17121426
[PubMed - indexed for MEDLINE]
Free Article
6.

Prenatal detection of subtelomeric rearrangements by multi-subtelomere FISH in a cohort of fetuses with major malformations.

Gignac J, Danis K, Tihy F, Lemyre E.

Am J Med Genet A. 2006 Dec 15;140(24):2768-75.

PMID:
17103433
[PubMed - indexed for MEDLINE]
7.

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 14;93(4):273-7.

PMID:
10946352
[PubMed - indexed for MEDLINE]
8.

Prenatal diagnosis of the distal 11q deletion and review of the literature.

Chen CP, Chern SR, Chang TY, Tzen CY, Lee CC, Chen WL, Chen LF, Wang W.

Prenat Diagn. 2004 Feb;24(2):130-6. Review.

PMID:
14974122
[PubMed - indexed for MEDLINE]
9.

Characterization of the human myeloid leukemia-derived cell line GF-D8 by multiplex fluorescence in situ hybridization, subtelomeric probes, and comparative genomic hybridization.

Tosi S, Giudici G, Rambaldi A, Scherer SW, Bray-Ward P, Dirscherl L, Biondi A, Kearney L.

Genes Chromosomes Cancer. 1999 Mar;24(3):213-21.

PMID:
10451701
[PubMed - indexed for MEDLINE]
10.

A de novo duplication of chromosome 21q22.11→qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings.

Chen CP, Huang HK, Ling PY, Su YN, Chen M, Tsai FJ, Wu PC, Chern SR, Chen YT, Lee CC, Wang W.

Taiwan J Obstet Gynecol. 2011 Dec;50(4):492-8. doi: 10.1016/j.tjog.2011.10.016.

PMID:
22212323
[PubMed - indexed for MEDLINE]
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. doi: 10.1159/000158519. Epub 2008 Sep 26.

PMID:
18818501
[PubMed - indexed for MEDLINE]
12.

Cryptic chromosome rearrangements detected by subtelomere assay in patients with mental retardation and dysmorphic features.

Dawson AJ, Putnam S, Schultz J, Riordan D, Prasad C, Greenberg CR, Chodirker BN, Mhanni AA, Chudley AE.

Clin Genet. 2002 Dec;62(6):488-94.

PMID:
12515261
[PubMed - indexed for MEDLINE]
13.

An assessment of the use of interphase FISH with chromosome specific probes as an alternative to cytogenetics in prenatal diagnosis.

Thein AT, Abdel-Fattah SA, Kyle PM, Soothill PW.

Prenat Diagn. 2000 Apr;20(4):275-80.

PMID:
10740198
[PubMed - indexed for MEDLINE]
14.

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.

PMID:
17100200
[PubMed - indexed for MEDLINE]
15.

Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.

Beaujard MP, Jouannic JM, Bessières B, Borie C, Martin-Luis I, Fallet-Bianco C, Portnoï MF.

Prenat Diagn. 2005 Jun;25(6):451-5.

PMID:
15966060
[PubMed - indexed for MEDLINE]
16.

De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.

Brisset S, Kasakyan S, L'Herminé AC, Mairovitz V, Gautier E, Aubry MC, Benkhalifa M, Tachdjian G.

Prenat Diagn. 2006 Mar;26(3):206-13.

PMID:
16450348
[PubMed - indexed for MEDLINE]
17.

Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction.

Chen CP, Chern SR, Chang TY, Lee CC, Chen LF, Tzen CY, Wang W, Lin CJ, Yang BP, Yang LS.

Prenat Diagn. 2003 Jan;23(1):40-3.

PMID:
12533811
[PubMed - indexed for MEDLINE]
18.

Prenatal cytogenetic abnormalities: correlations of structural rearrangements and ultrasonographically detected fetal anomalies.

Hume RF Jr, Kilmer-Ernst P, Wolfe HM, Ebrahim SA, Treadwell MC, Johnson MP, Evans MI.

Am J Obstet Gynecol. 1995 Oct;173(4):1334-6.

PMID:
7485349
[PubMed - indexed for MEDLINE]
19.

Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.

Lin CC, Hsieh YY, Wang CH, Li YC, Hsieh LJ, Lee CC, Tsai CH, Tsai FJ.

Prenat Diagn. 2006 Oct;26(10):898-902.

PMID:
16915592
[PubMed - indexed for MEDLINE]
20.

[Prenatal diagnosis of two pregnancies with risk of chromosomal disorders].

Cui YX, Huang B, Shi YC, Lu HY, Xia XY, Pan LJ, Huang YF.

Zhonghua Nan Ke Xue. 2007 Jul;13(7):624-7. Chinese.

PMID:
17725307
[PubMed - indexed for MEDLINE]

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