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Volumn 99, Issue 2, 1997, Pages 256-261

Nance-Horan syndrome: Linkage analysis in 4 families refines localization in Xp22.31-p22.13 region

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME XP; CLINICAL ARTICLE; CONGENITAL CATARACT; FACE MALFORMATION; GENE LOCATION; GENE MUTATION; GENE REARRANGEMENT; GENETIC LINKAGE; HAPLOTYPE; HUMAN; HUMAN CELL; MALE; PHENOTYPE; PRIORITY JOURNAL; TOOTH MALFORMATION;

EID: 0031033696     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004390050349     Document Type: Article
Times cited : (31)

References (17)
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    • Ballabio, A.1    Andria, G.2
  • 3
    • 0021241836 scopus 로고
    • The Nance-Horan syndrome: A rare X-linked ocular-dental trait with expression in heterozygous females
    • Bixler D, Higgins M, Hartsfield J (1984) The Nance-Horan syndrome: a rare X-linked ocular-dental trait with expression in heterozygous females. Clin Genet 26:30-35
    • (1984) Clin Genet , vol.26 , pp. 30-35
    • Bixler, D.1    Higgins, M.2    Hartsfield, J.3
  • 4
    • 0025201544 scopus 로고
    • Genetic localization and phenotypic expression of X-linked cataract (Xcat) in Mus musculus
    • Favor J, Pretsch W (1990) Genetic localization and phenotypic expression of X-linked cataract (Xcat) in Mus musculus. Genet Res 56:157-162
    • (1990) Genet Res , vol.56 , pp. 157-162
    • Favor, J.1    Pretsch, W.2
  • 6
    • 0016159688 scopus 로고
    • X-linked cataract and hutchinsonian teeth
    • Horan MB, Billson FA (1974) X-linked cataract and hutchinsonian teeth. Aust Pædiatr J 10:98-102
    • (1974) Aust Pædiatr J , vol.10 , pp. 98-102
    • Horan, M.B.1    Billson, F.A.2
  • 7
    • 0024942110 scopus 로고
    • Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: An appraisal of the Nance-Horan syndrome
    • Lewis RA (1989) Mapping the gene for X-linked cataracts and microcornea with facial, dental, and skeletal features to Xp22: an appraisal of the Nance-Horan syndrome. Trans Am Ophthalmol Soc 87:658-728
    • (1989) Trans Am Ophthalmol Soc , vol.87 , pp. 658-728
    • Lewis, R.A.1
  • 11
    • 0022320774 scopus 로고
    • The Nance-Horan syndrome of dental anomalies, congenital cataracts, microphthalmia, anteverted pinna: Case report
    • Seow WK, Brown JP, Romaniuk K (1985) The Nance-Horan syndrome of dental anomalies, congenital cataracts, microphthalmia, anteverted pinna: case report. Pediatr Dent 7:307-311
    • (1985) Pediatr Dent , vol.7 , pp. 307-311
    • Seow, W.K.1    Brown, J.P.2    Romaniuk, K.3
  • 12
    • 0025291429 scopus 로고
    • Nance-Horan syndrome: Localization within the region Xp21.1-Xp22.3 by linkage analysis
    • Stambolian D, Lewis RA, Buetow K, Bond A, Nussbaum R (1990) Nance-Horan syndrome: localization within the region Xp21.1-Xp22.3 by linkage analysis. Am J Hum Genet 47:13-19
    • (1990) Am J Hum Genet , vol.47 , pp. 13-19
    • Stambolian, D.1    Lewis, R.A.2    Buetow, K.3    Bond, A.4    Nussbaum, R.5
  • 13
    • 0028041410 scopus 로고
    • Mapping of the X-linked cataract (Xcat) mutation, the gene implicated in the Nance-Horan syndrome, on the mouse X chromosome
    • Stambolian D, Favor J, Silvers W, Avner Ph, Chapman V, Zhou E (1994) Mapping of the X-linked cataract (Xcat) mutation, the gene implicated in the Nance-Horan syndrome, on the mouse X chromosome. Genomics 22:377-380
    • (1994) Genomics , vol.22 , pp. 377-380
    • Stambolian, D.1    Favor, J.2    Silvers, W.3    Avner, Ph.4    Chapman, V.5    Zhou, E.6
  • 14
    • 0018342152 scopus 로고
    • A family with X-chromosomal recessive congenital cataract, microphthalmia, a peculiar form of the ear and dental anomalies
    • Van Dorp DB, Delleman JW (1979) A family with X-chromosomal recessive congenital cataract, microphthalmia, a peculiar form of the ear and dental anomalies. J Pediatr Ophthalmol Strabismus 16:166-171
    • (1979) J Pediatr Ophthalmol Strabismus , vol.16 , pp. 166-171
    • Van Dorp, D.B.1    Delleman, J.W.2
  • 16
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    • X-linked cataract and X-linked microphthalmos: How many deletion families?
    • Warburg M (1989) X-linked cataract and X-linked microphthalmos: how many deletion families? Am J Med Genet 34:451-453
    • (1989) Am J Med Genet , vol.34 , pp. 451-453
    • Warburg, M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.