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Volumn 131 A, Issue 1, 2004, Pages 99-100

Congenital heart defects associated with Smith-Magenis syndrome: Two cases of total anomalous pulmonary venous return [1]

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; CASE REPORT; CHILD; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CLINICAL FEATURE; CONGENITAL HEART MALFORMATION; ECHOCARDIOGRAPHY; FALLOT TETRALOGY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; KARYOTYPE; LETTER; LUNG VEIN DRAINAGE ANOMALY; MALE; PATENT DUCTUS ARTERIOSUS; PRIORITY JOURNAL; SMITH MAGENIS SYNDROME;

EID: 7244261868     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30290     Document Type: Letter
Times cited : (13)

References (18)
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  • 2
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    • Behjati F, Mullarkey M, Bergbaum A, Berry AC, Docherty Z. 1997. Chromosome deletion 17p11.2 (Smith-Magenis syndrome) in seven new patients, four of whom had been referred for fragile-X investigation. Clin Genet 51:71-74.
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  • 3
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  • 4
    • 0027160404 scopus 로고
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  • 6
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    • Interstitial deletion of 17p11.2 with brain abnormalities
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  • 7
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  • 8
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  • 13
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  • 15
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.