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Volumn 21, Issue 5, 2002, Pages 461-465

Sequence of right laterality with spleen: Widening the spectrum of heterotaxy

Author keywords

Asplenia polyesplenia syndrome; Heterotaxy; Laterality sequence; Right isomerism; Right laterality; Visceral situs anomalies

Indexed keywords

ACCESSORY SPLEEN; ARTICLE; ASPLENIA; AUTOPSY; CARDIOMEGALY; CASE REPORT; CYANOSIS; ECHOCARDIOGRAPHY; FEMALE; FETUS; HEART ARRHYTHMIA; HEPATOMEGALY; HETEROTAXY SYNDROME; HUMAN; HUMAN TISSUE; HYPOTENSION; NEWBORN; PRIORITY JOURNAL; STILLBIRTH;

EID: 0036744163     PISSN: 15227952     EISSN: None     Source Type: Journal    
DOI: 10.1080/15227950290104779     Document Type: Article
Times cited : (5)

References (16)
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    • Mutations of the connexin43 Gap-junction gene in patients with heart malformations and defects of laterality
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    • Britz-Cunningham, S.H.1    Shan, M.M.2    Zuppan, C.W.3    Fletcher, W.H.4
  • 5
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    • Mapping a gene for familial situs abnormalities to human chromosome Xq24-q27.1
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    • (1993) Nature Genet , vol.5 , pp. 403-407
    • Casey, B.1    Devoto, M.2    Jones, K.L.3    Ballabio, A.4
  • 9
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    • Human situs determination is probably controled by several different genes
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  • 11
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    • Asplenic syndrome in association with rudimentary spleen
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.