메뉴 건너뛰기




Volumn 23, Issue 6, 2003, Pages 666-667

Noonan syndrome: Diagnostic difficulties. A case report and literature review

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AMNIOCENTESIS; ANAMNESIS; APGAR SCORE; ASPIRATION; AUTOSOMAL DOMINANT DISORDER; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CESAREAN SECTION; CHILDBIRTH; CHROMOSOME REARRANGEMENT; CLINICAL FEATURE; COUNSELING; CRYPTORCHISM; CYSTIC LYMPHANGIOMA; DELIVERY; DIAGNOSTIC IMAGING; DIAGNOSTIC TEST; DISEASE ACTIVITY; DISEASE COURSE; FEMALE; FETUS GROWTH; GASTROSTOMY; GESTATION PERIOD; GROWTH RETARDATION; HEART DISEASE; HUMAN; HYDRAMNIOS; HYDROTHORAX; KARYOTYPE; KIDNEY DISEASE; MEDICAL DECISION MAKING; NOONAN SYNDROME; PREGNANCY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; PULMONARY VALVE; REVIEW; THROMBOCYTOPENIA; WEBBED NECK;

EID: 0344826510     PISSN: 01443615     EISSN: None     Source Type: Journal    
DOI: 10.1080/01443610310001607850     Document Type: Review
Times cited : (6)

References (12)
  • 2
    • 0015865133 scopus 로고
    • The Noonan syndrome - A review of the clinical and genetic features of 27 cases
    • Collins E. and Turner G. (1973) The Noonan syndrome - a review of the clinical and genetic features of 27 cases. Journal of Pediatrics, 83, 941-950.
    • (1973) Journal of Pediatrics , vol.83 , pp. 941-950
    • Collins, E.1    Turner, G.2
  • 5
    • 0034146751 scopus 로고    scopus 로고
    • Clinical utility of three-dimensional ultrasound
    • Downey D. B., Fenster A. and Williams J. C. (2000) Clinical utility of three-dimensional ultrasound. Radiographics, 20, 559-571.
    • (2000) Radiographics , vol.20 , pp. 559-571
    • Downey, D.B.1    Fenster, A.2    Williams, J.C.3
  • 11
    • 0034605374 scopus 로고    scopus 로고
    • Genetic heterogenicity in Noonan's syndrome: Evidence for autosomal recessive form
    • van der Burgt I. and Brunner H. (2000) Genetic heterogenicity in Noonan's syndrome: evidence for autosomal recessive form. American Journal of Medical Genetics, 94, 46-51.
    • (2000) American Journal of Medical Genetics , vol.94 , pp. 46-51
    • Van Der Burgt, I.1    Brunner, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.