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Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1.

(1996) JOURNAL OF MEDICAL GENETICS. 33(10). p.869-872
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Chicago
BERGEN, AAB, JB TENBRINK, F RIEMSLAG, EJM SCHUURMAN, Françoise Meire, M TIJMES, and PTVM DEJONG. 1996. “Conclusive Evidence for a Distinct Congenital Stationary Night Blindness Locus in Xp21.1.” Journal of Medical Genetics 33 (10): 869–872.
APA
BERGEN, A., TENBRINK, J., RIEMSLAG, F., SCHUURMAN, E., Meire, F., TIJMES, M., & DEJONG, P. (1996). Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1. JOURNAL OF MEDICAL GENETICS, 33(10), 869–872.
Vancouver
1.
BERGEN A, TENBRINK J, RIEMSLAG F, SCHUURMAN E, Meire F, TIJMES M, et al. Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1. JOURNAL OF MEDICAL GENETICS. 1996;33(10):869–72.
MLA
BERGEN, AAB, JB TENBRINK, F RIEMSLAG, et al. “Conclusive Evidence for a Distinct Congenital Stationary Night Blindness Locus in Xp21.1.” JOURNAL OF MEDICAL GENETICS 33.10 (1996): 869–872. Print.
@article{190760,
  author       = {BERGEN, AAB and TENBRINK, JB and RIEMSLAG, F and SCHUURMAN, EJM and Meire, Fran\c{c}oise and TIJMES, M and DEJONG, PTVM},
  issn         = {0022-2593},
  journal      = {JOURNAL OF MEDICAL GENETICS},
  language     = {eng},
  number       = {10},
  pages        = {869--872},
  title        = {Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1.},
  volume       = {33},
  year         = {1996},
}