INSITU GENETIC COMPLEMENTATION ANALYSIS OF DISORDERS WITH GENERALIZED PEROXISOMAL DYSFUNCTION

被引：0
|
作者：
STANLEY, WS [1 ]
SINGH, AK [1 ]
KULVATUNYOU, N [1 ]
SINGH, I [1 ]
机构：
[1] MED UNIV S CAROLINA,DEPT PATHOL & PEDIAT,CHARLESTON,SC 29425
来源：
CLINICAL RESEARCH | 1989年 / 37卷 / 02期
关键词：
D O I：
暂无
中图分类号：
R-3 [医学研究方法]; R3 [基础医学];
学科分类号：
1001 ;
摘要：
引用
收藏
页码：A832 / A832
页数：1
相关论文
共 50 条
  • [1] INSITU GENETIC COMPLEMENTATION ANALYSIS OF DISORDERS WITH GENERALIZED PEROXISOMAL DYSFUNCTION
    STANLEY, WS
    SINGH, AK
    KULVATUNYOU, N
    SINGH, I
    [J]. PEDIATRIC RESEARCH, 1989, 25 (04) : A146 - A146
  • [2] INSITU GENETIC COMPLEMENTATION ANALYSIS OF CELLS WITH GENERALIZED PEROXISOMAL DYSFUNCTION
    SINGH, AK
    KULVATUNYOU, N
    SINGH, I
    STANLEY, WS
    [J]. HUMAN HEREDITY, 1989, 39 (05) : 298 - 301
  • [3] GENETIC COMPLEMENTATION ANALYSIS IN PEROXISOMAL DISORDERS
    ROSCHER, A
    HOFLER, S
    HOFLER, G
    PASCHKE, E
    PALTAUF, F
    MOSER, A
    MOSER, H
    [J]. JOURNAL OF CLINICAL CHEMISTRY AND CLINICAL BIOCHEMISTRY, 1989, 27 (05): : 304 - 305
  • [4] GENETIC-HETEROGENEITY IN THE CEREBROHEPATORENAL (ZELLWEGER) SYNDROME AND OTHER INHERITED DISORDERS WITH A GENERALIZED IMPAIRMENT OF PEROXISOMAL FUNCTIONS - A STUDY USING COMPLEMENTATION ANALYSIS
    BRUL, S
    WESTERVELD, A
    STRIJLAND, A
    WANDERS, RJA
    SCHRAM, AW
    HEYMANS, HSA
    SCHUTGENS, RBH
    VANDENBOSCH, H
    TAGER, JM
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (06): : 1710 - 1715
  • [5] Hepatic dysfunction in peroxisomal disorders
    Baes, Myriam
    Van Veldhoven, Paul P.
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2016, 1863 (05): : 956 - 970
  • [6] PHYTANIC ACID ALPHA-OXIDATION AND COMPLEMENTATION ANALYSIS OF CLASSICAL REFSUM AND PEROXISOMAL DISORDERS
    POLLTHE, BT
    SKJELDAL, OH
    STOKKE, O
    POULOS, A
    DEMAUGRE, F
    SAUDUBRAY, JM
    [J]. HUMAN GENETICS, 1989, 81 (02) : 175 - 181
  • [7] PHENOTYPE OF PATIENTS WITH PEROXISOMAL DISORDERS SUBDIVIDED INTO 16 COMPLEMENTATION GROUPS
    MOSER, AB
    RASMUSSEN, M
    NAIDU, S
    WATKINS, PA
    MCGUINNESS, M
    HAJRA, AK
    CHEN, G
    RAYMOND, G
    LIU, A
    GORDON, D
    GARNAAS, K
    WALTON, DS
    SKJELDAL, OH
    GUGGENHEIM, MA
    JACKSON, LG
    ELIAS, ER
    MOSER, HW
    [J]. JOURNAL OF PEDIATRICS, 1995, 127 (01): : 13 - 22
  • [8] PHENOTYPIC RANGE OF GENERALIZED PEROXISOMAL DISORDERS
    NAIDU, S
    MOSER, AB
    MOSER, HW
    [J]. ANNALS OF NEUROLOGY, 1986, 20 (03) : 406 - 407
  • [9] COMPLEMENTATION STUDIES IN HUMAN GENETIC-DISORDERS - ANALYSIS OF HETEROGENEITY
    SPERLING, K
    [J]. BIOLOGISCHES ZENTRALBLATT, 1982, 101 (06): : 745 - 762
  • [10] High incidence of hyperoxaluria in generalized peroxisomal disorders
    Van Woerden, C.
    Poll-The, B.
    Wijburg, F.
    Duran, M.
    Wanders, R.
    Barth, P.
    Groothoff, J.
    [J]. PEDIATRIC NEPHROLOGY, 2007, 22 (09) : 1466 - 1466
12345