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Volumn 37, Issue 9, 2000, Pages 701-704

Interstitial deletion of chromosome 17 (del(17)(q22q23.3)) confirms a link with oesophageal atresia [2]

Author keywords

[No Author keywords available]

Indexed keywords

ANAMNESIS; BLOOD CULTURE; CASE REPORT; CHILD; CHROMOSOME 17; CLINICAL FEATURE; CONGENITAL MALFORMATION; DISEASE COURSE; ESOPHAGUS ATRESIA; GENE LOCUS; HUMAN; INTERSTITIAL CHROMOSOME DELETION; LETTER; MALE; PHYSICAL EXAMINATION; PRIORITY JOURNAL; TRACHEOESOPHAGEAL FISTULA;

EID: 0033828701     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter
Times cited : (51)

References (12)
  • 6
    • 0025797367 scopus 로고
    • Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal/duodenal atresia
    • (1991) J Med. Genet , vol.28 , pp. 389-394
    • Brunner, H.G.1    Winter, R.M.2
  • 7
    • 85142954725 scopus 로고
    • Catalogue of unbalanced chromosome aberrations in man
    • Berlin: De Gruyter
    • (1983) , pp. 854
    • Schinzel, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.