SCOPUS 정보 검색 플랫폼

Ophthalmic Genetics

Volumn 20, Issue 4, 1999, Pages 271-274

Conradi-Hunermann syndrome with ocular anomalies

(6) Tanaka, Yoko a Saitoh, Akira a Taniguchi, Hiroyasu a Oba, Keisuke a Kitaoka, Takashi a Amemiya, Tsugio a

a NAGASAKI UNIVERSITY (Japan)

Author keywords

Axenfeld Rieger syndrome; Conradi Hunermann syndrome; Developmental genes; Neural crest cell

Indexed keywords

ANTERIOR EYE SEGMENT; ARTICLE; CALCIFYING CHONDRODYSTROPHY; CASE REPORT; CHONDRODYSPLASIA PUNCTATA; CONGENITAL CATARACT; DISEASE ASSOCIATION; EYE MALFORMATION; FEMALE; HEREDITARY OPTIC ATROPHY; HOMEOBOX; HUMAN; INFANT; JAPAN; PRIORITY JOURNAL; RIEGER SYNDROME; CATARACT; CONGENITAL MALFORMATION; EYE DISEASE; OPTIC NERVE ATROPHY; PATHOLOGY; SYNDROME;

ANTERIOR EYE SEGMENT; CATARACT; CHONDRODYSPLASIA PUNCTATA; EYE DISEASES; FEMALE; HUMANS; INFANT; OPTIC ATROPHY; SYNDROME;

EID: 0033233171 PISSN: 13816810 EISSN: None Source Type: Journal
DOI: 10.1076/opge.20.4.271.2274 Document Type: Article

Times cited : (8)

References (10)

1
- 0016180122
- Case report. Case 1 (Conradi syndrome, autosomal dominant type)
- Feingold M, Bull MJ, Darling DB. Case report. Case 1 (Conradi syndrome, autosomal dominant type). Birth Defects Orig Artic Ser 1974;10: 93-99.
- (1974) Birth Defects Orig Artic Ser , vol.10 , pp. 93-99
- Feingold, M.¹ Bull, M.J.² Darling, D.B.³

2
- 0031750761
- X-linked dominant chondrodysplasia punctata: A peroxisomal disorder?
- Wilson CJ, Aftimos S. X-linked dominant chondrodysplasia punctata: a peroxisomal disorder? Am J Med Genet 1998;78(3):300-302.
- (1998) Am J Med Genet , vol.78 , Issue.3 , pp. 300-302
- Wilson, C.J.¹ Aftimos, S.²

3
- 0023262135
- Chondrodysplasia punctata
- Anderson PE Jr, Justesen P. Chondrodysplasia punctata. Skelet Radiol 1987;16:223-226.
- (1987) Skelet Radiol , vol.16 , pp. 223-226
- Anderson Jr., P.E.¹ Justesen, P.²

4
- 0011222227
- Peters' anomaly
- Ritch R, Schield MB, Krupin T, editors. St. Louis: The C.V. Mosby Comp
- Schottenstein EM. Peters' anomaly. In: Ritch R, Schield MB, Krupin T, editors. The Glaucoma, 2nd ed. St. Louis: The C.V. Mosby Comp, 1996; Vol. 2, 887-895.
- (1996) The Glaucoma, 2nd Ed. , vol.2 , pp. 887-895
- Schottenstein, E.M.¹

5
- 0020131388
- Waardenburg's syndrome
- Francois J. Waardenburg's syndrome. Int Ophthalmol 1982;5:3-13.
- (1982) Int Ophthalmol , vol.5 , pp. 3-13
- Francois, J.¹

6
- 0014981421
- Heterogeneity of chondrodysplasia punctata
- Spranger JW, Opitz JM, Bidder U. Heterogeneity of chondrodysplasia punctata. Humangenetik 1971;11: 190-212.
- (1971) Humangenetik , vol.11 , pp. 190-212
- Spranger, J.W.¹ Opitz, J.M.² Bidder, U.³

7
- 0025762432
- The peroxisome and the eye
- Steve JR, Jonathan DT. The peroxisome and the eye. Surv Ophthalmol 1991;35:353-368.
- (1991) Surv Ophthalmol , vol.35 , pp. 353-368
- Steve, J.R.¹ Jonathan, D.T.²

8
- 0343886304
- Lens
- Spencer WH, editor. Philadelphia: W.B. Saunders Comp
- Spencer WH. Lens. In: Spencer WH, editor. Ophthalmic Pathology, 3rd ed. Philadelphia: W.B. Saunders Comp, 1985; Vol. 1, 423-479.
- (1985) Ophthalmic Pathology, 3rd Ed. , vol.1 , pp. 423-479
- Spencer, W.H.¹

9
- 0003417727
- Boston: Little, Brown and Company
- Snell RS. Clinical Embryology for Students, 3rd ed. Boston: Little, Brown and Company, 1993.
- (1993) Clinical Embryology for Students, 3rd Ed.
- Snell, R.S.¹

10
- 0032254656
- Ocular malformations and developmental genes
- Traboulsi EI. Ocular malformations and developmental genes. J AAPOS 1998;2:317-323.
- (1998) J AAPOS , vol.2 , pp. 317-323
- Traboulsi, E.I.¹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.