Maumenee IH - Search Results

1

Linkage analysis in dominant optic atrophy.

Kivlin JD, Lovrien EW, Bishop DT, Maumenee IH. Kivlin JD, et al. Among authors: maumenee ih. Am J Hum Genet. 1983 Nov;35(6):1190-5. Am J Hum Genet. 1983. PMID: 6580816 Free PMC article.

2

Microphthalmos in the presumed homozygous offspring of a first cousin marriage and linkage analysis of a locus in a family with autosomal dominant cerulean congenital cataracts.

Bodker FS, Lavery MA, Mitchell TN, Lovrien EW, Maumenee IH. Bodker FS, et al. Among authors: maumenee ih. Am J Med Genet. 1990 Sep;37(1):54-9. doi: 10.1002/ajmg.1320370113. Am J Med Genet. 1990. PMID: 2240043

3

Linkage analysis in lattice corneal dystrophy.

Kivlin JD, Lovrien EW, Maumenee IH, Bishop DT, Bias W. Kivlin JD, et al. Among authors: maumenee ih. Am J Med Genet. 1984 Oct;19(2):387-90. doi: 10.1002/ajmg.1320190222. Am J Med Genet. 1984. PMID: 6334443

4

A second gene for cerulean cataracts maps to the beta crystallin region on chromosome 22.

Kramer P, Yount J, Mitchell T, LaMorticella D, Carrero-Valenzuela R, Lovrien E, Maumenee I, Litt M. Kramer P, et al. Genomics. 1996 Aug 1;35(3):539-42. doi: 10.1006/geno.1996.0395. Genomics. 1996. PMID: 8812489 Free article.

5

Fundus flavimaculatus without maculopathy. A clinicopathologic study.

McDonnell PJ, Kivlin JD, Maumenee IH, Green WR. McDonnell PJ, et al. Among authors: maumenee ih. Ophthalmology. 1986 Jan;93(1):116-9. doi: 10.1016/s0161-6420(86)33783-7. Ophthalmology. 1986. PMID: 3951808 Free article.

6

Assignment of the Nance-Horan syndrome to the distal short arm of the X chromosome.

Zhu D, Alcorn DM, Antonarakis SE, Levin LS, Huang PC, Mitchell TN, Warren AC, Maumenee IH. Zhu D, et al. Among authors: maumenee ih. Hum Genet. 1990 Nov;86(1):54-8. doi: 10.1007/BF00205172. Hum Genet. 1990. PMID: 1979306

7

Molecular genetics of human blue cone monochromacy.

Nathans J, Davenport CM, Maumenee IH, Lewis RA, Hejtmancik JF, Litt M, Lovrien E, Weleber R, Bachynski B, Zwas F, et al. Nathans J, et al. Among authors: maumenee ih. Science. 1989 Aug 25;245(4920):831-8. doi: 10.1126/science.2788922. Science. 1989. PMID: 2788922

8

Congenital motor nystagmus linked to Xq26-q27.

Kerrison JB, Vagefi MR, Barmada MM, Maumenee IH. Kerrison JB, et al. Among authors: maumenee ih. Am J Hum Genet. 1999 Feb;64(2):600-7. doi: 10.1086/302244. Am J Hum Genet. 1999. PMID: 9973299 Free PMC article.

9

Genetic heterogeneity of dominant optic atrophy, Kjer type: Identification of a second locus on chromosome 18q12.2-12.3.

Kerrison JB, Arnould VJ, Ferraz Sallum JM, Vagefi MR, Barmada MM, Li Y, Zhu D, Maumenee IH. Kerrison JB, et al. Among authors: maumenee ih. Arch Ophthalmol. 1999 Jun;117(6):805-10. doi: 10.1001/archopht.117.6.805. Arch Ophthalmol. 1999. PMID: 10369594

10

Identification of a locus (LCA9) for Leber's congenital amaurosis on chromosome 1p36.

Keen TJ, Mohamed MD, McKibbin M, Rashid Y, Jafri H, Maumenee IH, Inglehearn CF. Keen TJ, et al. Among authors: maumenee ih. Eur J Hum Genet. 2003 May;11(5):420-3. doi: 10.1038/sj.ejhg.5200981. Eur J Hum Genet. 2003. PMID: 12734549

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