SCOPUS 정보 검색 플랫폼

Ophthalmic Genetics

Volumn 21, Issue 4, 2000, Pages 227-233

Evidence for genetic heterogeneity in families with congenital motor nystagmus (CN)

(5) Oetting, W S a Armstrong, C M a Holleschau, A M a DeWan, A T a Summers, C G a

a UNIVERSITY OF MINNESOTA MEDICAL SCHOOL (United States)

Author keywords

Congenital nystagmus; Heterogeneity; Linkage; X linkage

Indexed keywords

ARTICLE; CHROMOSOME 6P; CHROMOSOME XP; CHROMOSOME XQ; CLINICAL ARTICLE; CONGENITAL NYSTAGMUS; DISEASE ASSOCIATION; FEMALE; GENETIC HETEROGENEITY; GENETIC LINKAGE; HETEROZYGOTE; HUMAN; MALE; PRIORITY JOURNAL; X CHROMOSOME LINKAGE;

CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 6; DNA; FAMILY; FEMALE; GENETIC HETEROGENEITY; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; MICROSATELLITE REPEATS; NYSTAGMUS, CONGENITAL; PEDIGREE; X CHROMOSOME;

EID: 0034486129 PISSN: 13816810 EISSN: None Source Type: Journal
DOI: 10.1076/1381-6810(200012)21:4;1-H;FT227 Document Type: Article

Times cited : (22)

References (21)

1
- 0025565654
- The clinical approach to the pediatric patient with nystagmus
- (1990) Int Pediatr , vol.5 , pp. 225-231
- Buckley, E.G.¹

2
- 0014045311
- Congenital nystagmus
- (1967) Can J Ophthalmol , vol.2 , pp. 4-10
- Cogan, D.G.¹

3
- 0023854835
- Congenital nystagmus: A clinical perspective in infancy
- (1988) Graefe's Arch Clin Exp Ophthalmol , vol.226 , pp. 178-180
- Gelbart, S.S.¹ Hoyt, C.S.²

4
- 0004207412
- New York: Springer-Verlag
- (1996) Pediatric Neuroophthalmology , pp. 302-325
- Brodsky, M.C.¹ Baker, R.S.² Hamed, L.M.³

5
- 0030001442
- A gene for autosomal dominant congenital nystagmus localizes to 6p12
- (1996) Genomics , vol.33 , pp. 523-526
- Kerrison, J.B.¹ Arnould, V.J.² Barmada, M.M.³ Koenekoop, R.K.⁴ Schmeckpeper, B.J.⁵ Maumenee, I.H.⁶

6
- 0031964691
- Clinical features of autosomal dominant congenital nystagmus linked to chromosome 6p12
- (1998) Am J Ophthalmol , vol.125 , pp. 64-70
- Kerrison, J.B.¹ Koenekoop, R.K.² Arnould, V.J.³ Maumenee, I.H.⁴

7
- 0033365220
- A gene for X-linked idiopathic congenital nystagmus (NYSI) maps to chromosome Xp11.4-p11.3
- (1999) Am J Hum Genet , vol.64 , pp. 1141-1146
- Cabot, A.¹ Rozet, J.-M.² Gerber, S.³ Perrault, I.⁴ Ducroq, D.⁵ Smahi, A.⁶ Souied, E.⁷ Munnich, A.⁸ Josseline, K.⁹

8
- 0033070051
- Congenital motor nystagmus linked to Xq26-q27
- (1999) Am J Hum Genet , vol.64 , pp. 600-607
- Kerrison, J.B.¹ Vagefi, M.R.² Barmada, M.M.³ Maumenee, I.H.⁴

9
- 0032446395
- Multiplexed short tandem repeat polymorphisms of the Weber 8A set of markers using tailed primers and infrared fluorescence detection
- (1998) Electrophoresis , vol.19 , pp. 3079-3083
- Oetting, W.S.¹ Armstrong, C.M.² Ronan, S.M.³ Young, T.L.⁴ Sellers, T.A.⁵ King, R.A.⁶

10
- 0032231941
- PedCheck: A program for identification of genotype incompatibilities in linkage analysis
- (1998) Am J Hum Genet , vol.63 , pp. 259-266
- O'Connell, J.R.¹ Weeks, D.E.²

11
- 0039513062
- Computer-simulation methods in human linkage analysis
- (1989) Proc Natl Acad Sci USA , vol.86 , pp. 4175-4178
- Ott, J.¹

12
- 0000801438
- SLINK: A general simulation program for linkage analysis
- (1990) Am J Hum Genet , vol.47 , Issue.SUPPL.
- Weeks, D.E.¹ Ott, J.² Lathrop, G.M.³

13
- 0027366195
- Faster sequential genetic linkage computations
- (1993) Am J Hum Genet , vol.53 , pp. 252-263
- Cottingham, R.W.¹ Idury, R.M.² Schaffer, A.A.³

14
- 0028260703
- Avoiding recomputation in genetic linkage analysis
- (1994) Hum Hered , vol.44 , pp. 225-237
- Schaffer, A.A.¹ Gupta, S.K.² Shiram, K.³ Cottingham, R.W.⁴

15
- 0021344005
- Easy calculations of LOD scores and genetic risks on small computers
- (1984) Am J Hum Genet , vol.36 , pp. 460-465
- Lathrop, G.M.¹ Lalouel, J.M.²

16
- 0342499587
- Strategies for multilocus analysis in humans
- (1984) Proc Natl Acad Sci U.S.A. , vol.81 , pp. 3443-3446
- Lathrop, G.M.¹ Lalouel, J.-M.² Julier, C.³ Ott, J.⁴

17
- 0022646961
- Construction of human genetic linkage maps: Likelihood calculations for multilocus analysis
- (1986) Genet Epidemiol , vol.3 , pp. 39-52
- Lathrop, G.M.¹ Lalouel, J.-M.² White, R.L.³

18
- 0029886532
- Parametric and non-parametric linkage analysis: A unified multipoint approach
- (1996) Am J Hum Genet , vol.58 , pp. 1347-1363
- Kruglyak, L.¹ Daly, M.J.² Reeve-Daly, M.P.³ Lander, E.S.⁴

19
- 0027493813
- Hereditary congenital nystagmus and gaze holding failure: The role of the neural integrator
- (1993) Neurology , vol.43 , pp. 1741-1749
- Dell'Osso, L.F.¹ Weissman, B.M.² Leigh, R.J.³ Abel, L.A.⁴ Sheth, N.V.⁵

20
- 0001269043
- A history of congenital stationary night blindness in nine consecutive generations
- (1907) Trans Ophthalmol Soc U.K. , vol.27 , pp. 269-293
- Nettleship, E.¹

21
- 0000991737
- A study of congenital nystagmus
- (1964) Acta Oto-laryngol , vol.57 , pp. 427-449
- Forssman, B.A.¹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.