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Archives of Ophthalmology
Volumn 126, Issue 3, 2008, Pages 431-432
Developmental glaucoma with chromosomal abnormalities of 9p deletion and 13q duplication
Author keywords

[No Author keywords available]
Indexed keywords

ANAMNESIS; CASE REPORT; CHROMOSOME 13Q; CHROMOSOME 9P; CHROMOSOME ABERRATION; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CLINICAL FEATURE; CORNEA EDEMA; GLAUCOMA; HUMAN; IN SITU HYBRIDIZATION; INFANT; INTRAOCULAR PRESSURE; KARYOTYPE; LETTER; MALE; MONOSOMY; NEWBORN; NUCLEAR MAGNETIC RESONANCE IMAGING; OPHTHALMOLOGY; PRIORITY JOURNAL; TRABECULOTOMY; TRISOMY 13;
EID: 40849097556     PISSN: 00039950     EISSN: 00039950     Source Type: Journal    
DOI: 10.1001/archopht.126.3.431     Document Type: Letter
Times cited : (6)
References (6)
  • 1
    • 0036976942 scopus 로고    scopus 로고
    • DNA sequence variants in the tyrosine-related protein 1 (TYRP1) gene are not associated with human pigmentary glaucoma
    • Lynch S, Yanagi G, DelBono E, Wiggs JL. DNA sequence variants in the tyrosine-related protein 1 (TYRP1) gene are not associated with human pigmentary glaucoma. Mol Vis. 2002;8:127-129.
    • (2002) Mol Vis , vol.8 , pp. 127-129
    • Lynch, S.1    Yanagi, G.2    DelBono, E.3    Wiggs, J.L.4
  • 2
    • 17844405571 scopus 로고    scopus 로고
    • Chromosomal abnormalities and glaucoma: A case of congenital glaucoma with trisomy 8q22-Qter/monosomy 9p23-Pter
    • Cohn AC, Kearns LS, Savarirayan R, Ryan J, Craig JE, Mackey DA. Chromosomal abnormalities and glaucoma: a case of congenital glaucoma with trisomy 8q22-Qter/monosomy 9p23-Pter. Ophthalmic Genet. 2005;26(1):45-53.
    • (2005) Ophthalmic Genet , vol.26 , Issue.1 , pp. 45-53
    • Cohn, A.C.1    Kearns, L.S.2    Savarirayan, R.3    Ryan, J.4    Craig, J.E.5    Mackey, D.A.6
  • 3
    • 0023305305 scopus 로고
    • Primary congenital glaucoma in a patient with trisomy 2q (q33-qter) and monosomy 9p (p24-pter)
    • Katsushima H, Kii T, Soma K, Ohyanagi K, Niikawa N. Primary congenital glaucoma in a patient with trisomy 2q (q33-qter) and monosomy 9p (p24-pter). Arch Ophthalmol. 1987;105(3):323-324.
    • (1987) Arch Ophthalmol , vol.105 , Issue.3 , pp. 323-324
    • Katsushima, H.1    Kii, T.2    Soma, K.3    Ohyanagi, K.4    Niikawa, N.5
  • 4
    • 84907115869 scopus 로고
    • Congenital glaucoma in a child with partial 1q duplication and 9p deletion
    • Verbraak FD, Pogány K, Pilon JW, et al. Congenital glaucoma in a child with partial 1q duplication and 9p deletion. Ophthalmic Paediatr Genet. 1992;13 (3):165-170.
    • (1992) Ophthalmic Paediatr Genet , vol.13 , Issue.3 , pp. 165-170
    • Verbraak, F.D.1    Pogány, K.2    Pilon, J.W.3
  • 5
    • 17544368015 scopus 로고    scopus 로고
    • Bunting R, Leitch J. Buphthalmos in trisomy 13. Eye. 2005;19(4):487-488.
    • Bunting R, Leitch J. Buphthalmos in trisomy 13. Eye. 2005;19(4):487-488.
  • 6
    • 17344372575 scopus 로고    scopus 로고
    • Mapping of a congenital microcoria locus to 13q31-32
    • Rouillac C, Roche O, Marchant D, et al. Mapping of a congenital microcoria locus to 13q31-32. Am J Hum Genet. 1998;62(5):1117-1122.
    • (1998) Am J Hum Genet , vol.62 , Issue.5 , pp. 1117-1122
    • Rouillac, C.1    Roche, O.2    Marchant, D.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.