SCOPUS 정보 검색 플랫폼

Volumn 104, Issue 5, 1999, Pages 410-411

Exclusion of RAI2 as the causative gene for Nance-Horan syndrome

(7) Walpole, Susannah M a Ronce, Nathalie b Grayson, Celene a Dessay, Benoît b Yates, John R W a Trump, Dorothy a Toutain, Annick b

a UNIVERSITY OF CAMBRIDGE (United Kingdom)

b CHU BRETONNEAU (France)

Author keywords

[No Author keywords available]

Indexed keywords

RETINOIC ACID;

ARTICLE; CLINICAL ARTICLE; CONGENITAL CATARACT; DEVELOPMENTAL DISORDER; GENE MAPPING; GENE SEQUENCE; HUMAN; MICROPHTHALMIA; PRIORITY JOURNAL; PROMOTER REGION; TOOTH MALFORMATION; X CHROMOSOME LINKED DISORDER;

ABNORMALITIES, MULTIPLE; ANIMALS; BASE SEQUENCE; CATARACT; CHROMOSOME MAPPING; CORNEA; DNA; FACE; HUMANS; LYMPHOCYTES; MENTAL RETARDATION; MICE; MICROPHTHALMOS; PROMOTER REGIONS (GENETICS); PROTEINS; SYNDROME; X CHROMOSOME;

EID: 0033033352 PISSN: 03406717 EISSN: None Source Type: Journal
DOI: 10.1007/s004390050976 Document Type: Article

Times cited : (10)

References (6)

1
- 0016159688
- X-linked cataract and Hutchinsonian teeth
- Horan M, Billson F (1974) X-linked cataract and Hutchinsonian teeth. Aust Paediat J 10:98-102
- (1974) Aust Paediat J , vol.10 , pp. 98-102
- Horan, M.¹ Billson, F.²

2
- 0016148082
- Congenital X-linked cataract, dental anomalies, and brachymetacarpalia
- Nance W, Warburg M, Bixler D, Helveston E (1974) Congenital X-linked cataract, dental anomalies, and brachymetacarpalia. Birth Defects 10:285-291
- (1974) Birth Defects , vol.10 , pp. 285-291
- Nance, W.¹ Warburg, M.² Bixler, D.³ Helveston, E.⁴

3
- 0031033696
- Nance-Horan syndrome: Linkage analysis in 4 families refines localization in Xp22.31-p22.13 region
- Toutain A, Ronce N, Dessay B, Robb L, Francannet C, Le Merrer M, Briard ML, Kaplan J, Moraine C (1997) Nance-Horan syndrome: linkage analysis in 4 families refines localization in Xp22.31-p22.13 region. Hum Genet 99:256-261
- (1997) Hum Genet , vol.99 , pp. 256-261
- Toutain, A.¹ Ronce, N.² Dessay, B.³ Robb, L.⁴ Francannet, C.⁵ Le Merrer, M.⁶ Briard, M.L.⁷ Kaplan, J.⁸ Moraine, C.⁹

4
- 0031572304
- High-resolution physical map of the X-linked retinoschisis interval in Xp22
- Walpole SM, Nicolaou A, Howell GR, Whittaker A, Bentley DR, Ross MT, Yates JRW, Trump D (1997) High-resolution physical map of the X-linked retinoschisis interval in Xp22. Genomics 44:300-308
- (1997) Genomics , vol.44 , pp. 300-308
- Walpole, S.M.¹ Nicolaou, A.² Howell, G.R.³ Whittaker, A.⁴ Bentley, D.R.⁵ Ross, M.T.⁶ Yates, J.R.W.⁷ Trump, D.⁸

5
- 0033082273
- Identification and characterization of the human homologue (RA12) of a mouse retinoic acid-induced gene in Xp22
- Walpole SM, Hiriyana KT, Nicolaou A, Bingham EL, Durham J, Vaudin M, Ross MT, Yates JRW, Sieving PA, Trump D (1998) Identification and characterization of the human homologue (RA12) of a mouse retinoic acid-induced gene in Xp22. Genomics 55:275-283
- (1998) Genomics , vol.55 , pp. 275-283
- Walpole, S.M.¹ Hiriyana, K.T.² Nicolaou, A.³ Bingham, E.L.⁴ Durham, J.⁵ Vaudin, M.⁶ Ross, M.T.⁷ Yates, J.R.W.⁸ Sieving, P.A.⁹ Trump, D.¹⁰

6
- 25744471500
- Refined mapping of the Nance-Horan syndrome to a 2 cM region on Xp22.2
- Zhu D, Li Y, Traboulsi E, Mitchell T, Maumenee I (1998) Refined mapping of the Nance-Horan syndrome to a 2 cM region on Xp22.2. Am J Med Genet 63:A317
- (1998) Am J Med Genet , vol.63
- Zhu, D.¹ Li, Y.² Traboulsi, E.³ Mitchell, T.⁴ Maumenee, I.⁵

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.