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Items: 1 to 20 of 118

1.

Fluorescence in situ hybridization in prenatal screening: lessons from an inherited chromosome 18 marker.

Valentin M, Ottenwalter A, Serero S, Muller F, Luton D, Ducarme G.

Prenat Diagn. 2009 Dec;29(12):1177-9. doi: 10.1002/pd.2381. No abstract available.

PMID:
19816880
2.

False-positive prenatal diagnosis of trisomy 18 by interphase FISH: hybridization of chromosome 18 alpha-satellite DNA probe (D18Z1) to the heterochromatic region of chromosome 9.

Wei S, Siu VM, Decker A, Quigg MH, Roberson J, Xu J, Adeyinka A.

Prenat Diagn. 2007 Nov;27(11):1064-6. No abstract available.

PMID:
17654752
3.

Fluorescence in situ hybridization for prenatal screening of chromosomal aneuploidies.

Weise A, Liehr T.

Expert Rev Mol Diagn. 2008 Jul;8(4):355-7. doi: 10.1586/14737159.8.4.355. Review. No abstract available.

PMID:
18598216
4.

Application of fluorescent in situ hybridization for 'de novo' anomalies in prenatal diagnosis.

Van Opstal D, Eussen HJ, Van Hemel JO, Sachs ES.

Prenat Diagn. 1993 Sep;13(9):825-32.

PMID:
8278313
5.

Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter).

Chen CP, Lin SP, Lin CC, Li YC, Hsieh LJ, Chern SR, Lee CC, Chen YJ, Wang W.

Prenat Diagn. 2005 Dec;25(12):1170-2. No abstract available.

PMID:
16315335
6.
7.

Prenatal diagnosis of partial 2p trisomy by 'de novo' duplication 2p (13.1-->21). Confirmation by FISH.

Siffroi JP, Molina-Gomez D, Viguie F, Nessmann C, Dadoune JP.

Prenat Diagn. 1994 Nov;14(11):1097-9. No abstract available.

PMID:
7877961
8.

False-positive prenatal diagnosis of trisomy 18 by interphase FISH: hybridization of chromosome 18 alpha-satellite probe (D18Z1) to chromosome 2.

Collin A, Sladkevicius P, Soller M.

Prenat Diagn. 2009 Dec;29(13):1279-81. doi: 10.1002/pd.2401. No abstract available.

PMID:
19911414
9.

Molecular cytogenetic characterization of marker chromosomes found at prenatal diagnosis.

Verschraegen-Spae MR, van Roy N, de Perdigo A, de Paepe A, Speleman F.

Prenat Diagn. 1993 May;13(5):385-94.

PMID:
8341637
10.

Detection of confined placental mosaicism in trisomy 18 conceptions using interphase cytogenetic analysis.

Harrison KJ, Barrett IJ, Lomax BL, Kuchinka BD, Kalousek DK.

Hum Genet. 1993 Oct;92(4):353-8.

PMID:
8225315
11.

Rapid prenatal diagnosis by AmnioPCR and AmnioFISH: routine testing for Down's syndrome (trisomy 21) and sex chromosome trisomies, but targeted testing for Edward's (trisomy 18) and Patau's syndromes (trisomy 13).

Su LL, Biswas A, Ho SS, Ponnusamy S, Kothandaraman N, Chia D, Choolani M.

Ann Acad Med Singapore. 2004 Sep;33(5 Suppl):S53-4. No abstract available.

PMID:
15651208
12.

Genetic counselling in a prenatal marker chromosome identified as an i (18p) by in situ hybridization.

Darnaude MT, Diaz de Bustamante A, Cabello P, Vallcorba I.

Ann Genet. 1996;39(2):61-3.

PMID:
8766134
13.

[Application of spectral karyotyping in diagnosis and prenatal diagnosis of the marker chromosome].

Liao C, Pan M, Li DZ, Yi CX, Hu SY, Yuan SM, Wu SQ.

Zhonghua Fu Chan Ke Za Zhi. 2008 May;43(5):321-4. Chinese.

PMID:
18953861
14.

Prenatal diagnosis of complete sole trisomy 1q.

Pettenati MJ, Berry M, Shashi V, Hartley Bowen J, Harper M.

Prenat Diagn. 2001 Jun;21(6):435-40. Review.

PMID:
11438944
15.

[A case of 18-trisomy diagnosed by fluorescence in situ hybridization of amniocyte].

Maruyama H, Fukushi Y, Tando T, Wada J, Niino T, Sato S, Kagiya A, Sato S, Saito Y.

Nihon Sanka Fujinka Gakkai Zasshi. 1994 Jul;46(7):611-3. Japanese. No abstract available.

PMID:
8089600
16.
17.

Appraisal of fluorescence in situ hybridization (FISH) techniques in prenatal diagnosis.

Grao P, Guitart M, Coll MD, Egozcue J.

Early Hum Dev. 1993 Jun;33(2):101-8.

PMID:
8055774
19.

Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH).

Witters I, Devriendt K, Legius E, Matthijs G, Van Schoubroeck D, Van Assche FA, Fryns JP.

Prenat Diagn. 2002 Jan;22(1):29-33.

PMID:
11810646
20.

M-FISH applications in clinical genetics.

Cetin Z, Berker Karaüzüm S, Yakut S, Mihçi E, Baumer A, Wey E, Taçoy S, Bağci G, Lüleci G.

Genet Couns. 2005;16(3):257-68.

PMID:
16259323

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