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Volumn 76, Issue 6, 1996, Pages 548-549

Isomerism of the atrial appendages associated with 22q11 deletion in a fetus

Author keywords

atrial isomerism; chromosome 22q11; fetal karyotype; microdeletion

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 22Q; CHROMOSOME DAMAGE; FEMALE; FETUS; HEART ATRIUM; HEART DISEASE; HUMAN; ISOMERISM; KARYOTYPE; PRIORITY JOURNAL;

EID: 0030446465     PISSN: 13556037     EISSN: None     Source Type: Journal    
DOI: 10.1136/hrt.76.6.548     Document Type: Article
Times cited : (19)

References (10)
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  • 2
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  • 3
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  • 4
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    • Mutations of the connexion 43 gap junction gene in patients with heart malformations and detects of laterality
    • Britz-Cunningham SH, Shah MM, Zuppan CW, Fletcher WH. Mutations of the connexion 43 gap junction gene in patients with heart malformations and detects of laterality. N Engl J Med 1995;332:1323-9.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.