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Volumn 92, Issue 3, 2000, Pages 166-169

Imperforate anus in Feingold syndrome

Author keywords

Brachydactyly; Duodenal atresia; Esophageal atresia; Microcephaly; Syndactyly

Indexed keywords

ADULT; ANUS ATRESIA; ARTICLE; BRACHYDACTYLY; CASE REPORT; CLINICAL FEATURE; DISEASE ASSOCIATION; DUODENUM ATRESIA; ESOPHAGUS ATRESIA; FEMALE; FINGER MALFORMATION; HUMAN; INFANT; MALE; MICROCEPHALY; PEDIGREE ANALYSIS; PRIORITY JOURNAL; SYNDACTYLY;

EID: 0342369582     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(sici)1096-8628(20000529)92:3<166::aid-ajmg2>3.0.co;2-%23     Document Type: Article
Times cited : (12)

References (11)
  • 2
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    • Brunner HG, Winter RM. 1991. Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability. J Med Genet 28:389-394.
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    • Brunner, H.G.1    Winter, R.M.2
  • 5
    • 0003593937 scopus 로고
    • Case report 30
    • Feingold M. 1975. Case report 30. Synd Ident 3:16-17.
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    • Feingold, M.1
  • 6
    • 0017838162 scopus 로고
    • An unusual microcephaly
    • Feingold M. 1978. An unusual microcephaly. Hosp Pract 13:44-49.
    • (1978) Hosp Pract , vol.13 , pp. 44-49
    • Feingold, M.1
  • 7
    • 0031002838 scopus 로고    scopus 로고
    • Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay
    • Feingold M, Hall BD, Lacassie Y, Martínez-Frías ML. 1997. Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay. Am J Med Genet 69:245-249.
    • (1997) Am J Med Genet , vol.69 , pp. 245-249
    • Feingold, M.1    Hall, B.D.2    Lacassie, Y.3    Martínez-Frías, M.L.4
  • 9
    • 0013692119 scopus 로고
    • Tracheo-esophageal fistula/esophageal atresia multiple congenital anomaly syndrome: Feingold type
    • Hall BD. 1994. Tracheo-esophageal fistula/esophageal atresia multiple congenital anomaly syndrome: Feingold type. Proc Greenwood Genet Center 13:123-124.
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    • Hall, B.D.1
  • 10
    • 0025042565 scopus 로고
    • Microcephaly, mesobrachyphalangy, and tracheoesophageal fistula: MMT syndrome
    • König R, Selzer G, Stolp A, Fuchs S. 1990. Microcephaly, mesobrachyphalangy, and tracheoesophageal fistula: MMT syndrome. Dysmorph Clin Genet 4:83-86.
    • (1990) Dysmorph Clin Genet , vol.4 , pp. 83-86
    • König, R.1    Selzer, G.2    Stolp, A.3    Fuchs, S.4
  • 11
    • 85080491697 scopus 로고    scopus 로고
    • MIM 112800, MIM 243150
    • Online Mendelian Inheritance in Man (OMIM). http//www.ncbi. nlm.nih.gov/Omim (MIM 112800, MIM 243150).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.