AN XX MALE WITH 21-HYDROXYLASE DEFICIENCY

被引:0
|
作者
BARNES, ND [1 ]
机构
[1] ADDENBROOKES HOSP,DEPT PAEDIAT,CAMBRIDGE CB2 2QQ,ENGLAND
关键词
D O I
暂无
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
引用
收藏
页码:79 / 79
页数:1
相关论文
共 50 条
  • [21] LOCATION OF THE GENE FOR 21-HYDROXYLASE DEFICIENCY
    PUCHOLT, V
    FITZSIMMONS, JS
    REYNOLDS, MA
    GELSTHORPE, K
    [J]. PEDIATRIC RESEARCH, 1979, 13 (10) : 1186 - 1186
  • [22] DETECTION OF HETEROZYGOTE OF 21-HYDROXYLASE DEFICIENCY
    LEVINE, LS
    PANG, S
    DUPONT, B
    POLLACK, M
    LORENZEN, F
    NEW, MI
    [J]. LANCET, 1980, 1 (8168): : 603 - 604
  • [23] Clinical outcomes in 21-hydroxylase deficiency
    Nordenstrom, Anna
    Lajic, Svetlana
    Falhammar, Henrik
    [J]. CURRENT OPINION IN ENDOCRINOLOGY DIABETES AND OBESITY, 2021, 28 (03) : 318 - 324
  • [24] Kawasaki syndrome and 21-hydroxylase deficiency
    Hazeki, Daisuke
    Nomura, Yuichi
    Mizota, Michiyo
    Yotsumoto, Keiko
    Nonaka, Yukiko
    Tanabe, Takayuki
    Kawano, Yoshifumi
    [J]. PEDIATRICS INTERNATIONAL, 2008, 50 (01) : 119 - 120
  • [25] MOLECULAR PATHOLOGY OF 21-HYDROXYLASE DEFICIENCY
    STRACHAN, T
    [J]. JOURNAL OF INHERITED METABOLIC DISEASE, 1994, 17 (04) : 430 - 441
  • [26] Prenatal counselling of 21-hydroxylase deficiency
    Huidobro Fernandez, B.
    Roldan Martin, M. B.
    Rodriguez Arnao, M. D.
    Ezquieta Zubicaray, B.
    [J]. ANALES DE PEDIATRIA, 2012, 76 (01): : 51 - 52
  • [27] The genetics of steroid 21-hydroxylase deficiency
    Speiser, PW
    [J]. ENDOCRINOLOGIST, 2005, 15 (01): : 37 - 43
  • [28] Molecular Genetics of 21-Hydroxylase Deficiency
    Wedell, Anna
    [J]. PEDIATRIC ADRENAL DISEASES, 2011, 20 : 80 - 87
  • [29] DETECTION OF HETEROZYGOTE OF 21-HYDROXYLASE DEFICIENCY
    SOBEL, DO
    GUTAI, JP
    JONES, JC
    WAGENER, DK
    SMITH, W
    [J]. LANCET, 1980, 1 (8158): : 47 - 47
  • [30] RECENT ADVANCES IN 21-HYDROXYLASE DEFICIENCY
    NEW, MI
    LEVINE, LS
    [J]. ANNUAL REVIEW OF MEDICINE, 1984, 35 : 649 - 663