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Volumn 10, Issue 3, 2000, Pages 233-234

Guess what! Trichorhinophalangeal syndrome type I

Author keywords

[No Author keywords available]

Indexed keywords

ALOPECIA; ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHILD; DIAGNOSTIC APPROACH ROUTE; DIFFERENTIAL DIAGNOSIS; DIGITAL RADIOGRAPHY; ELLIS VAN CREVELD SYNDROME; FEMALE; HAIR; HUMAN; HUMAN CELL; HUMAN TISSUE; LARSEN SYNDROME; LONG PHILTRUM; MANDIBLE HYPOPLASIA; SKIN APPENDAGE DISEASE; SYSTEMIC DISEASE; TRICHORHINOPHALENGEAL SYNDROME TYPE I; CHONDRODYSPLASIA; GENETICS; PATHOLOGY;

EID: 0033624098     PISSN: 11671122     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (1)

References (9)
  • 3
    • 0030983732 scopus 로고    scopus 로고
    • The trichorhinophalangeal syndromes: Frequency and parental origin of 8q deletions
    • 3. Nardman J, Tranebjaerg L, Horsthemke B, Ludecke HJ. The trichorhinophalangeal syndromes: frequency and parental origin of 8q deletions. Hum Genet 1997; 99: 638-43.
    • (1997) Hum Genet , vol.99 , pp. 638-643
    • Nardman, J.1    Tranebjaerg, L.2    Horsthemke, B.3    Ludecke, H.J.4
  • 4
    • 0013972535 scopus 로고
    • Das tricho-rhino-phalangeale syndrom
    • 4. Giedion AA. Das tricho-rhino-phalangeale Syndrom. Helv Paediatr Acta 1966; 21: 475-82.
    • (1966) Helv Paediatr Acta , vol.21 , pp. 475-482
    • Giedion, A.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.