Congenital bilateral absence of the vas deferens and recombination at CFTR

被引:0
|
作者
David Haig
机构
[1] Harvard University,Department of Organismic and Evolutionary Biology
来源
关键词
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
页码:801 / 801
相关论文
共 50 条
  • [21] CONGENITAL BILATERAL ABSENCE OF THE VAS-DEFERENS - EXHAUSTIVE SCREENING FOR MUTATIONS IN THE 27 EXONS OF THE CFTR GENE
    MERCIER, B
    LISSENS, W
    AUDREZET, MP
    BONDUELLE, M
    QUERE, I
    VERLINGUE, C
    RAGUENES, O
    LIEBAERS, I
    FEREC, C
    AMERICAN JOURNAL OF HUMAN GENETICS, 1993, 53 (03) : 1203 - 1203
  • [22] Identification of the second CFTR mutation in patients with congenital bilateral absence of vas deferens undergoing ART protocols
    Giuliani, Rossella
    Antonucci, Ivana
    Torrente, Isabella
    Grammatico, Paola
    Palka, Giandomenico
    Stuppia, Liborio
    ASIAN JOURNAL OF ANDROLOGY, 2010, 12 (06) : 819 - 826
  • [23] Molecular diagnosis of congenital bilateral absence of the vas deferens: Analyses of the CFTR gene in 64 French patients
    Bienvenu, T
    Adjiman, M
    Thiounn, N
    Jeanpierre, M
    Hubert, D
    Lepercq, J
    Francoual, C
    Wolf, JP
    Izard, V
    Jouannet, P
    Kaplan, JC
    Beldjord, C
    ANNALES DE GENETIQUE, 1997, 40 (01): : 5 - 9
  • [24] Molecular screening of CFTR gene in Egyptian patients with congenital bilateral absence of the vas deferens: a preliminary study
    Fathy, M.
    Ramzy, T.
    Elmonem, M. A.
    Amer, M.
    Zeidan, A.
    Hassan, F. A.
    Mehaney, D. A.
    ANDROLOGIA, 2016, 48 (10) : 1307 - 1312
  • [25] Congenital bilateral absence of vas deferens with a new missense mutation (P499A) in the CFTR gene
    Arduino, C
    Ferrone, M
    Brusco, A
    Garnerone, S
    Fontana, D
    Rolle, L
    Carbonara, AO
    CLINICAL GENETICS, 1998, 53 (03) : 202 - 204
  • [26] Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens
    T. Dörk
    Bernd Dworniczak
    Christa Aulehla-Scholz
    Dagmar Wieczorek
    Ingolf Böhm
    Antonia Mayerova
    Hans H. Seydewitz
    Eberhard Nieschlag
    Dieter Meschede
    Jürgen Horst
    Hans-Jürgen Pander
    Herbert Sperling
    Felix Ratjen
    Eberhard Passarge
    Jörg Schmidtke
    Manfred Stuhrmann
    Human Genetics, 1997, 100 : 365 - 377
  • [27] Distinct spectrum of CFTR gene mutations in congenital absence of vas deferens
    Dork, T
    Dworniczak, B
    AulehlaScholz, C
    Wieczorek, D
    Bohm, I
    Mayerova, A
    Seydewitz, HH
    Nieschlag, E
    Meschede, D
    Horst, J
    Pander, HJ
    Sperling, H
    Ratjen, F
    Passarge, E
    Schmidtke, J
    Stuhrmann, M
    HUMAN GENETICS, 1997, 100 (3-4) : 365 - 377
  • [28] Testicular CFTR splice variants in patients with congenital absence of the vas deferens
    Larriba, S
    Bassas, L
    Gimenez, J
    Ramos, MD
    Segura, A
    Nunes, V
    Estivill, X
    Casals, T
    HUMAN MOLECULAR GENETICS, 1998, 7 (11) : 1739 - 1744
  • [29] CFTR GENE VARIANT FOR PATIENTS WITH CONGENITAL ABSENCE OF VAS-DEFERENS
    ZIELENSKI, J
    PATRIZIO, P
    COREY, M
    HANDELIN, B
    MARKIEWICZ, D
    ASCH, R
    TSUI, LC
    AMERICAN JOURNAL OF HUMAN GENETICS, 1995, 57 (04) : 958 - 960
  • [30] Airway inflammation and infection in congenital bilateral absence of the vas deferens
    Gilljam, M
    Moltyaner, Y
    Downey, GP
    Devlin, R
    Durie, P
    Cantin, AM
    Zielenski, J
    Tullis, DE
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2004, 169 (02) : 174 - 179