Application of fluorescence in situ hybridization in prenatal diagnosis for identification of rare structural aberration.

被引：0

作者：

Pawlowska, B

Ilnicka, A

Bogdanowicz, J

Tomankiewicz-Zawadzka, A

Roszkowski, T

Zaremba, J

机构：

[1] Inst Psychiat & Neurol, Warsaw, Poland

[2] Clin Obstet & Gynecol, Warsaw, Poland

来源：

EUROPEAN JOURNAL OF HUMAN GENETICS | 2002年 / 10卷

关键词：

D O I：

暂无

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：282 / 282

页数：1

共 50 条

[11] Application of fluorescence in situ hybridization to the identification of different marker chromosomes
Verschraegen-Spae, MR
Quack, B
Rousseaux, S
Pison, H
Messiaen, L
De Paepe, A
Lespinasse, J
ANNALES DE GENETIQUE, 1998, 41 (01): : 5 - 10
[12] IDENTIFICATION OF A MARKER CHROMOSOME BY FLUORESCENCE INSITU HYBRIDIZATION (FISH) IN PRENATAL-DIAGNOSIS
TRAN, TN
HORN, E
CUI, MY
YING, KL
TRICHE, TJ
FALK, RE
AMERICAN JOURNAL OF HUMAN GENETICS, 1991, 49 (04) : 308 - 308
[13] Defining the role of fluorescence in situ hybridization on uncultured amniocytes for prenatal diagnosis of aneuploidies - Discussion
Elias, S
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1997, 176 (04) : 774 - 774
[14] Prenatal diagnosis of mosaic tetrasomy 21q confirmed by fluorescence in situ hybridization
Nagarsheth, NP
Mootabar, H
CLINICAL GENETICS, 1997, 51 (04) : 260 - 263
[15] PRENATAL-DIAGNOSIS OF CAT EYE SYNDROME BY FLUORESCENCE IN-SITU HYBRIDIZATION (FISH)
DRISCOLL, DA
SELLINGER, B
BUDARF, ML
EMANUEL, BS
MILLER, RC
DONNENFELD, AE
REESER, SL
AMERICAN JOURNAL OF HUMAN GENETICS, 1993, 53 (03) : 1401 - 1401
[16] Clinical application of fluorescence in situ hybridization in the diagnosis and management of melanocytic lesions
Nijhawan, Rajiv I.
Votava, Henry J.
Mariwalla, Kavita
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2013, 68 (04) : AB150 - AB150
[17] Fluorescence in situ hybridization for prenatal screening of chromosomal aneuploidies
Weise, Anja
Liehr, Thomas
EXPERT REVIEW OF MOLECULAR DIAGNOSTICS, 2008, 8 (04) : 355 - 357
[18] Rapid prenatal diagnosis aneuploidy from uncultured amniotic fluid cells by fluorescence 'in situ' hybridization
Leite, RP
Criado, B
EUROPEAN JOURNAL OF HUMAN GENETICS, 1998, 6 : 90 - 90
[19] Residual risk for cytogenetic abnormalities after prenatal diagnosis by interphase fluorescence in situ hybridization (FISH)
Homer, J
Bhatt, S
Huang, B
Thangavelu, M
PRENATAL DIAGNOSIS, 2003, 23 (07) : 566 - 571
[20] Prenatal diagnosis of supernumerary marker chromosome using traditional banding and fluorescence in situ hybridization techniques
Bagci, G
Acar, H
Alper, Ö
Tomruk, H
Lüleci, G
CYTOGENETICS AND CELL GENETICS, 1999, 85 (1-2): : 138 - 138

← 1 2 3 4 5 →