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Volumn 130, Issue 5, 1997, Pages 822-824

Ivemark syndrome with asplenia in siblings

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ASPLENIA; AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; ECHOCARDIOGRAPHY; FEMALE; FETUS; FETUS ECHOGRAPHY; HUMAN; LUNG LOBE; LUNG MALFORMATION; MALE; NEWBORN; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SIBLING;

EID: 0030862398     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(97)80028-5     Document Type: Article
Times cited : (27)

References (10)
  • 1
    • 85119465176 scopus 로고
    • VA McKusick Mendelian inheritance in man [CD-ROM] September 29, 1995 Johns Hopkins University Baltimore
    • (1995)
    • McKusick, VA1
  • 2
    • 0015807315 scopus 로고
    • Familial occurence of Ivemark syndrome with splenic hypoplasia and asplenia in sibs
    • J Simpson H Yellweger Familial occurence of Ivemark syndrome with splenic hypoplasia and asplenia in sibs J Med Genet 10 1973 303 304
    • (1973) J Med Genet , vol.10 , pp. 303-304
    • Simpson, J1    Yellweger, H2
  • 3
    • 0016840564 scopus 로고
    • Syndromes of asplenia and polysplenia: a review of cardiac and noncardiac malformations in 60 cases with special reference to diagnosis and prognosis
    • V Rose T Izukawa CAF Moes Syndromes of asplenia and polysplenia: a review of cardiac and noncardiac malformations in 60 cases with special reference to diagnosis and prognosis Br Heart J 37 1975 840 852
    • (1975) Br Heart J , vol.37 , pp. 840-852
    • Rose, V1    Izukawa, T2    Moes, CAF3
  • 4
    • 0029060788 scopus 로고
    • Mutaions of connexin-43 gap junction gene in patients with heart malformations and defects of laterality
    • SH Britz-Cunningham MM Shah CW Zuppan WH Fltecher Mutaions of connexin-43 gap junction gene in patients with heart malformations and defects of laterality N Engl J Med 332 1995 1323 1329
    • (1995) N Engl J Med , vol.332 , pp. 1323-1329
    • Britz-Cunningham, SH1    Shah, MM2    Zuppan, CW3    Fltecher, WH4
  • 5
    • 0002236198 scopus 로고
    • Implications of agenesis of spleen on the pathogenesis of cono-truncus anomalies in childhood
    • BI Ivemark Implications of agenesis of spleen on the pathogenesis of cono-truncus anomalies in childhood Acta Paediatr 44 104 1955 1 110
    • (1955) Acta Paediatr , vol.44 , Issue.104 , pp. 1-110
    • Ivemark, BI1
  • 8
    • 0027454207 scopus 로고
    • Mapping a gene for familial situs abnormalites to human chromosome Xq24-q27.1
    • B Casey M Devoto KL Jones A Ballabino Mapping a gene for familial situs abnormalites to human chromosome Xq24-q27.1 Nat Genet 5 1993 403 407
    • (1993) Nat Genet , vol.5 , pp. 403-407
    • Casey, B1    Devoto, M2    Jones, KL3    Ballabino, A4
  • 9
    • 0026707667 scopus 로고
    • Human situs determination is probably controlled by several different genes
    • R Carmi JA Boughman KR Rosenbaum Human situs determination is probably controlled by several different genes Am J Med Genet 44 1992 246 249
    • (1992) Am J Med Genet , vol.44 , pp. 246-249
    • Carmi, R1    Boughman, JA2    Rosenbaum, KR3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.