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Volumn 11, Issue 3, 2002, Pages 155-161

Hemifacial microsomia, external auditory canal atresia, deafness and Mullerian anomalies associated with acro-osteolysis: A new autosomal recessive syndrome?

Author keywords

Acro osteolysis; Atresia auditory canal; Deafness; Goldenhar syndrome; Hemifacial microsomia; Mullerian anomalies

Indexed keywords

ACROOSTEOLYSIS; ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CONSANGUINITY; DIFFERENTIAL DIAGNOSIS; EAR MALFORMATION; EXTERNAL EAR CANAL ATRESIA; FEMALE; GOLDENHAR SYNDROME; HEARING IMPAIRMENT; HEMIFACIAL MICROSOMIA; HUMAN; KIDNEY AGENESIS; MALE; MUELLERIAN DUCT; PRIORITY JOURNAL; SYNDROME VATER; AUDITORY CANAL; CASE REPORT; CONGENITAL MALFORMATION; FACE; GENETICS; MIDDLE AGED; MULTIPLE MALFORMATION SYNDROME; PATHOLOGY; PEDIGREE; RECESSIVE GENE;

EID: 0036018122     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200207000-00001     Document Type: Article
Times cited : (19)

References (10)
  • 3
    • 0001578146 scopus 로고
    • Associations malformatives de l'oeil et de l'oreille en particulare, le syndrome dermoide epibulbaire-appendices auriculares-fistula auris congenita et ses relations avec la dysotose mandibulo-faciale
    • (1952) J Genet Hum , vol.1 , pp. 243
    • Goldenhar, M.1
  • 8
    • 0014769389 scopus 로고
    • A second family with renal, vaginal and middle ear anomalies
    • (1970) J Pediatr , vol.76 , pp. 641
    • Turner, G.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.