PRESYMPTOMATIC AND PRENATAL TESTING IN HUNTINGTON DISEASE - REPLY

被引：2
|
作者：
SHAW, MW
机构：
来源：
AMERICAN JOURNAL OF MEDICAL GENETICS | 1987年 / 28卷 / 03期
关键词：
D O I：
10.1002/ajmg.1320280330
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：765 / 766
页数：2
相关论文
共 50 条
  • [41] PRESYMPTOMATIC TESTING FOR HUNTINGTON CHOREA - ETHICAL AND LEGAL ISSUES
    LAMPORT, AT
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1987, 26 (02): : 307 - 314
  • [42] United Kingdom experience with presymptomatic testing of individuals at 25% risk for Huntington's disease
    Benjamin, CM
    Lashwood, A
    CLINICAL GENETICS, 2000, 58 (01) : 41 - 49
  • [43] Prenatal testing in Huntington disease: after the test, choices recommence
    Hanane Bouchghoul
    Stéphane-Françoise Clément
    Danièle Vauthier
    Cécile Cazeneuve
    Sandrine Noel
    Marc Dommergues
    Delphine Héron
    Jacky Nizard
    Marcela Gargiulo
    Alexandra Durr
    European Journal of Human Genetics, 2016, 24 : 1535 - 1540
  • [44] Prenatal Genetic Testing for Huntington's Disease: Ethical Considerations
    Ashtiani, Setareh
    Doonanco, Jasmine
    Suchowersky, Oksana
    NEUROTHERAPEUTICS, 2018, 15 (01) : 234 - 235
  • [45] Experience with the presymptomatic diagnosis of Huntington's disease
    Lucotte, G
    Aouizerate, A
    Gerard, N
    Mercier, G
    Turpin, JC
    SEMAINE DES HOPITAUX, 1997, 73 (15-16): : 504 - 508
  • [46] PRENATAL, PRESYMPTOMATIC, AND DIAGNOSTIC TESTING WITH DIRECT MUTATION ANALYSIS IN HUNTINGTONS-DISEASE
    ROSSER, E
    HUSON, SM
    NORBURY, G
    LANCET, 1994, 343 (8895): : 487 - 488
  • [47] Prenatal testing in Huntington disease: after the test, choices recommence
    Bouchghoul, Hanane
    Clement, Stephane-Francoise
    Vauthier, Daniele
    Cazeneuve, Cecile
    Noel, Sandrine
    Dommergues, Marc
    Heron, Delphine
    Nizard, Jacky
    Gargiulo, Marcela
    Durr, Alexandra
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2016, 24 (11) : 1535 - 1540
  • [48] Prenatal testing for Huntington's disease:: a European collaborative study
    Simpson, SA
    Zoeteweij, MW
    Nys, K
    Harper, P
    Dürr, A
    Jacopini, G
    Yapijakis, C
    Evers-Kiebooms, G
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2002, 10 (11) : 689 - 693
  • [49] Prenatal testing for Huntington's disease: a European collaborative study
    Sheila A Simpson
    Moniek W Zoeteweij
    Kurt Nys
    Peter Harper
    Alexandra Dürr
    Gioia Jacopini
    Christos Yapijakis
    Gerry Evers-Kiebooms
    European Journal of Human Genetics, 2002, 10 : 689 - 693
  • [50] The search for sensitive biomarkers in presymptomatic Huntington disease
    Henry, Pierre-Gilles
    Mochel, Fanny
    JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2012, 32 (05): : 769 - 770
12345