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Volumn 99, Issue 2, 2005, Pages 207-211

A previously unreported association between Nance-Horan syndrome and spontaneous dental abscesses

Author keywords

[No Author keywords available]

Indexed keywords

ABSCESS; ARTICLE; CASE REPORT; CLINICAL FEATURE; CONGENITAL CATARACT; FEMALE; GENETICS; HUMAN; INCISOR; NANCE HORAN SYNDROME; PHENOTYPE; SCHOOL CHILD; TOOTH MALFORMATION; X CHROMOSOME LINKED DISORDER;

EID: 12344298179     PISSN: 10792104     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tripleo.2004.07.004     Document Type: Article
Times cited : (24)

References (14)
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  • 2
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    • A family with X-chromosomal recessive congenital cataract, micropthalmia, a peculiar form of the ear and dental anomalies
    • D.B. Van Dorp, and J.W. Delleman A family with X-chromosomal recessive congenital cataract, micropthalmia, a peculiar form of the ear and dental anomalies J Pediatr Ophthalmol Strabismus 16 1979 166 171
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    • Van Dorp, D.B.1    Delleman, J.W.2
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    • 12344267309 scopus 로고
    • Pedigree of hereditary cataract, illustrating sex-limited type
    • F.B. Walsh, and M.E. Wegman Pedigree of hereditary cataract, illustrating sex-limited type Bull Johns Hopkins Hosp 61 1937 125 135
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    • Walsh, F.B.1    Wegman, M.E.2
  • 6
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  • 7
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    • Nance-Horan syndrome: Linkage analysis in 4 families refines localization in Xp22.31-p22.13 region
    • A. Toutain, N. Ronce, and B. Dessay Nance-Horan syndrome: linkage analysis in 4 families refines localization in Xp22.31-p22.13 region Hum Genet 99 1997 256 261
    • (1997) Hum Genet , vol.99 , pp. 256-261
    • Toutain, A.1    Ronce, N.2    Dessay, B.3
  • 8
    • 0029262286 scopus 로고
    • Nance-Horan syndrome: A contiguous gene syndrome involving deletion of the amelogenin gene? a case report and molecular analysis
    • E. Franco, S. Hodgson, N. Lench, and G.J. Roberts Nance-Horan syndrome: a contiguous gene syndrome involving deletion of the amelogenin gene? A case report and molecular analysis Oral Dis 1 1995 8 11
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  • 10
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    • Micropthalmia with linear skin defects (MLS) syndrome: Clinical, cytogenetic and molecular characterization
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.