Improvement of preimplantation genetic diagnosis (PGD) for the cystic fibrosis mutation ΔF508 by fluorescent polymerase chain reaction

被引：0
|
作者：
Moutou, C
Viville, S
机构：
[1] CHRU, Serv Diagnost Genet, Fac Med, Strasbourg, France
[2] ULP, INSERM, CNRS, Inst Genet & Biol Mol, F-67404 Strasbourg, France
[3] CMCO, SIHCUS, Serv Biol Reprod, F-67303 Schiltigheim, France
来源：
PRENATAL DIAGNOSIS | 1999年 / 19卷 / 13期
关键词：
D O I：
10.1002/(SICI)1097-0223(199912)19:13<1248::AID-PD737>3.3.CO;2-7
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：1248 / 1250
页数：3
相关论文
共 50 条
  • [1] Preimplantation genetic diagnosis of cystic fibrosis (Delta F508)
    Ao, A
    Handyside, A
    Winston, RML
    EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 1996, 65 (01): : 7 - 10
  • [2] Clinical experience with preimplantation genetic diagnosis of cystic fibrosis (delta F508)
    Ao, A
    Ray, P
    Harper, J
    Lesko, J
    Paraschos, T
    Atkinson, G
    Soussis, I
    Taylor, D
    Handyside, A
    Hughes, M
    Winston, RML
    PRENATAL DIAGNOSIS, 1996, 16 (02) : 137 - 142
  • [3] Generation of a human embryonic stem cell line encoding the cystic fibrosis mutation ΔF508, using preimplantation genetic diagnosis
    Pickering, SJ
    Minger, SL
    Patel, M
    Taylor, H
    Black, C
    Burns, CJ
    Ekonomou, A
    Braude, PR
    REPRODUCTIVE BIOMEDICINE ONLINE, 2005, 10 (03) : 390 - 397
  • [4] OPTIMAL POLYMERASE CHAIN-REACTION AMPLIFICATION FOR PREIMPLANTATION DIAGNOSIS IN CYSTIC-FIBROSIS (DELTA-F508)
    CUI, KH
    HAAN, EA
    WANG, LJ
    MATTHEWS, CD
    BRITISH MEDICAL JOURNAL, 1995, 311 (7004): : 536 - 540
  • [5] Restoration of function of the ΔF508 mutation in cystic fibrosis
    Rowan, Stephen
    THORAX, 2012, 67 (10) : 881 - 881
  • [6] Phenotypic variability of cystic fibrosis: case report of twins with F508/F508 mutation
    Fernanda Hernandez-Amaris, Maria
    Maria Gomez-Vasquez, Ana
    Pachajoa H, Harry
    REVISTA CHILENA DE PEDIATRIA-CHILE, 2014, 85 (04): : 470 - 475
  • [7] Characterization of ΔF508/F508C embryos for preimplantation genetic diagnosis
    Giménez, C
    Pérez, N
    Egozcue, J
    Vidal, F
    Boada, M
    Veiga, A
    Santaló, J
    HUMAN REPRODUCTION, 1999, 14 : 238 - 238
  • [8] Cystic fibrosis in Argentina: The frequency of the Delta F508 mutation
    Luna, MC
    Granados, PA
    Olek, K
    Pivetta, OH
    HUMAN GENETICS, 1996, 97 (03) : 314 - 314
  • [9] The delta F508 mutation in cystic fibrosis and impact on sinus development
    Woodworth, Bradford A.
    Ahn, Chadwick
    Flume, Patrick A.
    Schlosser, Rodney J.
    AMERICAN JOURNAL OF RHINOLOGY, 2007, 21 (01): : 122 - 127
  • [10] Neonatal screening for the cystic fibrosis main mutation ΔF508 in Estonia
    Klaassen, T
    Teder, M
    Viikmaa, M
    Metspalu, A
    JOURNAL OF MEDICAL SCREENING, 1998, 5 (01) : 16 - 19
12345