Crossref journal-article
Wiley
Clinical Genetics (311)
Bibliography

Shastry, B., Hejtmancik, J., Hiraoka, M., Ibaraki, N., Okubo, Y., Okubo, A., Han, D., & Trese, M. (2000). Linkage and candidate gene analysis of autosomal‐dominant familial exudative vitreoretinopathy. Clinical Genetics, 58(4), 329–332. Portico.

Authors 8
  1. BS Shastry (first)
  2. JF Hejtmancik (additional)
  3. M Hiraoka (additional)
  4. N Ibaraki (additional)
  5. Y Okubo (additional)
  6. A Okubo (additional)
  7. DP Han (additional)
  8. MT Trese (additional)
References 19 Referenced 10
  1. 10.1016/0002-9394(69)91237-9
  2. {'key': 'e_1_2_3_3_2', 'first-page': '211', 'article-title': 'Familial exudative vitreoretinopathy', 'volume': '79', 'author': 'Tasman W', 'year': '1981', 'journal-title': 'Trans Am Ophthalmol Soc'} / Trans Am Ophthalmol Soc / Familial exudative vitreoretinopathy by Tasman W (1981)
  3. 10.1007/BF00681132
  4. 10.1002/(sici)1096-8628(19970317)69:2<217::aid-ajmg19>3.0.co;2-o
  5. 10.1034/j.1399-0004.1998.5440409.x
  6. 10.1016/S0002-9394(14)73977-7
  7. 10.1136/bjo.77.3.168
  8. {'key': 'e_1_2_3_9_2', 'first-page': '749', 'article-title': 'The autosomal dominant exudative vitreoretinopathy locus maps on 11q and is closely linked to D11S 533', 'volume': '51', 'author': 'Li Y', 'year': '1992', 'journal-title': 'Am J Hum Genet'} / Am J Hum Genet / The autosomal dominant exudative vitreoretinopathy locus maps on 11q and is closely linked to D11S 533 by Li Y (1992)
  9. 10.3109/13816819609057871
  10. 10.1038/ng1093-180
  11. 10.1006/geno.1995.1052
  12. 10.1006/geno.1997.4863
  13. 10.1002/(SICI)1098-1004(1997)9:5<396::AID-HUMU3>3.0.CO;2-2
  14. 10.1073/pnas.81.11.3443
  15. {'key': 'e_1_2_3_16_2', 'first-page': '95', 'article-title': 'Refining the locus for Best vitelliform macular dystrophy and mutation analysis of the candidate gene ROM1', 'volume': '54', 'author': 'Nicholos BE', 'year': '1994', 'journal-title': 'Am J Hum Genet'} / Am J Hum Genet / Refining the locus for Best vitelliform macular dystrophy and mutation analysis of the candidate gene ROM1 by Nicholos BE (1994)
  16. 10.1001/archopht.1997.01100150653015
  17. {'key': 'e_1_2_3_18_2', 'first-page': 'S565', 'article-title': 'Identification of a new Norrie disease gene mutation in an African‐American infant with advanced retinopathy of prematurity', 'volume': '40', 'author': 'Buffenn AN', 'year': '1999', 'journal-title': 'Invest Ophthalmol Vis Sci'} / Invest Ophthalmol Vis Sci / Identification of a new Norrie disease gene mutation in an African‐American infant with advanced retinopathy of prematurity by Buffenn AN (1999)
  18. 10.1016/S0002-9394(14)72661-3
  19. 10.1093/hmg/1.9.685
Dates
Type When
Created 22 years, 5 months ago (March 11, 2003, 6:25 a.m.)
Deposited 1 year, 10 months ago (Oct. 29, 2023, 6:10 a.m.)
Indexed 1 year, 8 months ago (Dec. 19, 2023, 2:56 p.m.)
Issued 24 years, 11 months ago (Oct. 1, 2000)
Published 24 years, 11 months ago (Oct. 1, 2000)
Published Online 23 years, 8 months ago (Dec. 24, 2001)
Published Print 24 years, 11 months ago (Oct. 1, 2000)
Funders 0

None

@article{Shastry_2000, title={Linkage and candidate gene analysis of autosomal‐dominant familial exudative vitreoretinopathy}, volume={58}, ISSN={1399-0004}, url={http://dx.doi.org/10.1034/j.1399-0004.2000.580412.x}, DOI={10.1034/j.1399-0004.2000.580412.x}, number={4}, journal={Clinical Genetics}, publisher={Wiley}, author={Shastry, BS and Hejtmancik, JF and Hiraoka, M and Ibaraki, N and Okubo, Y and Okubo, A and Han, DP and Trese, MT}, year={2000}, month=oct, pages={329–332} }