메뉴 건너뛰기




Volumn 9, Issue 2, 2000, Pages 111-114

Severe short stature, hyperphalangy of the index fingers, mental retardation and facial dysmorphism

Author keywords

Autosomal recessive; Hyperphalangism; Skeletal dysplasia

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CONSANGUINITY; FACE DYSMORPHIA; FINGER MALFORMATION; HUMAN; MALE; MENTAL RETARDATION MALFORMATION SYNDROME; PRIORITY JOURNAL; SHORT STATURE; SYNDROME DELINEATION;

EID: 0034116988     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200009020-00007     Document Type: Article
Times cited : (5)

References (10)
  • 1
    • 0031026099 scopus 로고    scopus 로고
    • Unusual type of brachydactyly associated with intraventricular septal defect and deafness: A new condition?
    • Camera G, Costa M (1997). Unusual type of brachydactyly associated with intraventricular septal defect and deafness: a new condition? Clin Dysmorphol 6:31-33.
    • (1997) Clin Dysmorphol , vol.6 , pp. 31-33
    • Camera, G.1    Costa, M.2
  • 3
    • 0000935499 scopus 로고
    • Nanisme chondrodystrophique avec ossification anarchique et polymalformations chez deux soeurs
    • Desbuquois G, Grenier B, Michel J, Rossignol C (1966). Nanisme chondrodystrophique avec ossification anarchique et polymalformations chez deux soeurs. Arch Fr Pediatr 23:573-587.
    • (1966) Arch Fr Pediatr , vol.23 , pp. 573-587
    • Desbuquois, G.1    Grenier, B.2    Michel, J.3    Rossignol, C.4
  • 5
    • 0002930114 scopus 로고
    • The occurrence of congenital keratoconus posticus circumscriptus
    • Haney WP, Falls HF (1961). The occurrence of congenital keratoconus posticus circumscriptus. Am J Ophthalmol 51/52:53-57.
    • (1961) Am J Ophthalmol , vol.51-52 , pp. 53-57
    • Haney, W.P.1    Falls, H.F.2
  • 8
    • 0031773746 scopus 로고    scopus 로고
    • A new multiple congenital anomaly, mental retardation syndrome with preaxial polydactyly, hyperphalangism, deafness and orodental anomalies
    • Temtamy SA, Meguid NA, Ismail SI, Ramzy MI (1998). A new multiple congenital anomaly, mental retardation syndrome with preaxial polydactyly, hyperphalangism, deafness and orodental anomalies. Clin Dysmorphol 7: 249-255.
    • (1998) Clin Dysmorphol , vol.7 , pp. 249-255
    • Temtamy, S.A.1    Meguid, N.A.2    Ismail, S.I.3    Ramzy, M.I.4
  • 9
    • 0027417358 scopus 로고
    • Index finger hyperphalangy and multiple anomalies: Catel-Manzke syndrome?
    • Wilson GN, King TE, Brookshire GS (1993). Index finger hyperphalangy and multiple anomalies: Catel-Manzke syndrome? Am J Med Genet 46:176-179.
    • (1993) Am J Med Genet , vol.46 , pp. 176-179
    • Wilson, G.N.1    King, T.E.2    Brookshire, G.S.3
  • 10
    • 0024268878 scopus 로고
    • Different manifestations of hyperphalangism
    • Wood VE (1988). Different manifestations of hyperphalangism. J Hand Surg 13A:883-887.
    • (1988) J Hand Surg , vol.13 A , pp. 883-887
    • Wood, V.E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.