FAMILIAL STUDY IN NOONAN SYNDROME

被引:0
|
作者
CORTES, R [1 ]
ARMENDARES, S [1 ]
机构
[1] INST MEXICANO SEGURO SOCIAL, DIV INVEST GENET HUMANA, SUBJEFATURA INVEST CLIN, MEXICO CITY 73, MEXICO
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
下载
收藏
页码:90 / 91
页数:2
相关论文
共 50 条
  • [1] FAMILIAL OCCURRENCE OF NOONAN SYNDROME
    QAZI, QH
    ARNON, RG
    PAYDAR, MH
    MAPA, HC
    AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1974, 127 (05): : 696 - 698
  • [2] New mutation in NRAS in familial Noonan syndrome
    Zuniga, A.
    Pedrola, L.
    Castillo, L.
    Aller, E.
    Pi, G.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2018, 26 : 489 - 489
  • [3] Bilateral kidney duplication in familial Noonan's syndrome
    Barker, M
    Engelhardt, W
    CLINICAL PEDIATRICS, 2001, 40 (04) : 241 - 242
  • [4] NOONAN SYNDROME - FAMILY STUDY
    BOLTON, MR
    PUGH, DM
    MATTIOLI, LF
    DUNN, MI
    SCHIMKE, RN
    ANNALS OF INTERNAL MEDICINE, 1974, 80 (05) : 626 - 629
  • [5] Mutation in NRAS in familial Noonan syndrome - case report and review of the literature
    Ekvall, Sara
    Wilbe, Maria
    Dahlgren, Jovanna
    Legius, Eric
    van Haeringen, Arie
    Westphal, Otto
    Anneren, Goran
    Bondeson, Marie-Louise
    BMC MEDICAL GENETICS, 2015, 16
  • [6] A CLINICAL-STUDY OF NOONAN SYNDROME
    SHARLAND, M
    BURCH, M
    MCKENNA, WM
    PATON, MA
    ARCHIVES OF DISEASE IN CHILDHOOD, 1992, 67 (02) : 178 - 183
  • [7] Clinical and molecular study of the Noonan syndrome
    Cammarata-Scalisi, Francisco
    Neri, Giovanni
    Grazia Pomponi, Maria
    Mancano, Giorgia
    Da Silva, Gloria
    Avendano, Andrea
    Angelina Lacruz-Rengel, Maria
    Stock, Frances
    Sosa, Angel
    INVESTIGACION CLINICA, 2012, 53 (04): : 395 - 401
  • [8] A case of Noonan syndrome with unusual clinical severity and familial factor XII deficiency
    Ghirri, P
    Vuerich, M
    Fantoni, M
    Cuttano, A
    Merusi, I
    Ciulli, C
    Bottone, U
    Boldrini, A
    PRENATAL AND NEONATAL MEDICINE, 2000, 5 (03): : 193 - 196
  • [9] Noonan syndrome
    Roberts, Amy E.
    Allanson, Judith E.
    Tartaglia, Marco
    Gelb, Bruce D.
    LANCET, 2013, 381 (9863): : 333 - 342
  • [10] NOONAN SYNDROME
    DAOUD, MS
    DAHL, PR
    SU, WPD
    SEMINARS IN DERMATOLOGY, 1995, 14 (02): : 140 - 144