메뉴 건너뛰기




Volumn 16, Issue 1, 1999, Pages 0029-0032

Prader-Willi syndrome associated with fetal goiter: A case report

Author keywords

Fetal goiter; Hypotonia; Neonatal thyroid abnormalities; Prader Willi Syndrome; Thrombocytopenia

Indexed keywords

ARTICLE; CASE REPORT; CLINICAL FEATURE; DISEASE ASSOCIATION; FETUS; GOITER; HUMAN; INFANT; MALE; MUSCLE HYPOTONIA; PRADER WILLI SYNDROME; PRIORITY JOURNAL; THROMBOCYTOPENIA; THYROID DISEASE; ADULT; ECHOGRAPHY; FEMALE; FETUS DISEASE; FLUORESCENCE IN SITU HYBRIDIZATION; FOLLOW UP; GENETICS; NEWBORN; PREGNANCY;

EID: 0032604518     PISSN: 07351631     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-993832     Document Type: Article
Times cited : (17)

References (8)
  • 1
    • 0000927260 scopus 로고
    • Ein syndrom von adipositas kleinwuchs, kryptorchismus und oligophrenie nach myatonieartigem im neugeborenenalter
    • Prader A, Labhart A, Willi H. Ein syndrom von adipositas kleinwuchs, kryptorchismus und oligophrenie nach myatonieartigem im neugeborenenalter. Schweiz Med Wochenschr 1956;86:1260-1261
    • (1956) Schweiz Med Wochenschr , vol.86 , pp. 1260-1261
    • Prader, A.1    Labhart, A.2    Willi, H.3
  • 2
    • 0027476507 scopus 로고
    • Cytogenetic and molecular studies in the Prader-Willi and Angelman syndromes: An overview
    • Knoll JH, Wagstaff J, Lalande M. Cytogenetic and molecular studies in the Prader-Willi and Angelman syndromes: An overview. Am J Med Genetics 1993;46:2-6
    • (1993) Am J Med Genetics , vol.46 , pp. 2-6
    • Knoll, J.H.1    Wagstaff, J.2    Lalande, M.3
  • 4
    • 0026595355 scopus 로고
    • Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13
    • Dittrich B, Robinson WP, et al. Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13. Hum Genetics 1990;90:313-15
    • (1990) Hum Genetics , vol.90 , pp. 313-315
    • Dittrich, B.1    Robinson, W.P.2
  • 5
    • 0027473988 scopus 로고
    • Multiplex PCR of three nucleotide repeats in the Prader-Willi/Angelman critical region (15q11-13): Molecular diagnosis and mechanism of uniparental disomy
    • Mutirangura A, Greenberg F, et al. Multiplex PCR of three nucleotide repeats in the Prader-Willi/Angelman critical region (15q11-13): Molecular diagnosis and mechanism of uniparental disomy. Hum Mol Genetics 1993;2:143-151
    • (1993) Hum Mol Genetics , vol.2 , pp. 143-151
    • Mutirangura, A.1    Greenberg, F.2
  • 7
    • 0021950748 scopus 로고
    • Leukaemia and the Prader-Willi syndrome
    • Hall B. Leukaemia and the Prader-Willi syndrome. Lancet 1985;1:46
    • (1985) Lancet , vol.1 , pp. 46
    • Hall, B.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.