SCOPUS 정보 검색 플랫폼

Ophthalmic Genetics

Volumn 28, Issue 2, 2007, Pages 69-72

Chromosomal abnormalities and glaucoma: A case of congenital glaucoma associated with 9p deletion syndrome

(4) Saha, Konal a Lloyd, Ian Christopher a Russell Eggitt, Isabelle Mary b Taylor, David Samuel Irving b

a MANCHESTER ROYAL EYE HOSPITAL (United Kingdom)

b HOSPITAL FOR SICK CHILDREN (United Kingdom)

Author keywords

9p; Chromosomal; Congenital; Deletion; Glaucoma

Indexed keywords

CASE REPORT; CHROMOSOME DELETION; CHROMOSOME DELETION 9; DISEASE ASSOCIATION; FEMALE; GENETIC DISORDER; GLAUCOMA; HUMAN; INFANT; LITERATURE; MEDLINE; PRIORITY JOURNAL; REVIEW;

CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 9; FEMALE; GLAUCOMA; HUMANS; INFANT; KARYOTYPING; SYNDROME;

EID: 34250186472 PISSN: 13816810 EISSN: 17445094 Source Type: Journal
DOI: 10.1080/13816810701351339 Document Type: Review

Times cited : (3)

References (7)

1
- 0023734622
- Eleven New cases of del (9p) and features from 80 cases
- Huret JL, Leonard C, Forestier G, Rethore MO, Lejeune J. Eleven New cases of del (9p) and features from 80 cases. J Med Genet. 1988;25:741-749.
- (1988) J Med Genet , vol.25 , pp. 741-749
- Huret, J.L.¹ Leonard, C.² Forestier, G.³ Rethore, M.O.⁴ Lejeune, J.⁵

2
- 0020584303
- Congenital glaucoma and other ocular abnormalities associated with pericentric inversion of Chromosone 11
- Broughton WL, Rosebaum KN, Beauchamp GR. Congenital glaucoma and other ocular abnormalities associated with pericentric inversion of Chromosone 11. Arch Ophthalmol. 1983;101:594-597.
- (1983) Arch Ophthalmol , vol.101 , pp. 594-597
- Broughton, W.L.¹ Rosebaum, K.N.² Beauchamp, G.R.³

3
- 0003597161
- 4th ed. Philadelphia: WB Saunders
- Smith DW. Recognizable patterns of human malformation (genetic embryologic and clinical aspects), 4th ed. Philadelphia: WB Saunders, 1988;44-45.
- (1988) Recognizable patterns of human malformation (genetic embryologic and clinical aspects) , pp. 44-45
- Smith, D.W.¹

4
- 0023305305
- 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;105:323-324.
- (1987) Arch Ophthalmol , vol.105 , pp. 323-324
- Katsushima, H.¹ Kii, T.² Soma, K.³ Ohyanagi, K.⁴ Niikawa, N.⁵

5
- 84907115869
- Congenital glaucoma in a child with partial 1q duplication and 9p deletion
- Verbraak FD, Pogany K, Pillon JW, Mooy CM, De France HF, Hennekam RCM, Bleeker-Wagemakers EM. Congenital glaucoma in a child with partial 1q duplication and 9p deletion. Ophthalm Paed Genet. 1992;13:165-170.
- (1992) Ophthalm Paed Genet , vol.13 , pp. 165-170
- Verbraak, F.D.¹ Pogany, K.² Pillon, J.W.³ Mooy, C.M.⁴ De France, H.F.⁵ Hennekam, R.C.M.⁶ Bleeker-Wagemakers, E.M.⁷

6
- 0015260684
- Pericentre inversions of chromosone 9 in two families
- Wahram J, Atidia J, Goitein R, Cohen T. Pericentre inversions of chromosone 9 in two families. Cytogenet Cell Genet. 1972;11:132-144.
- (1972) Cytogenet Cell Genet , vol.11 , pp. 132-144
- Wahram, J.¹ Atidia, J.² Goitein, R.³ Cohen, T.⁴

7
- 17844405571
- 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

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.