LOD scores, location scores, and X-linked cone dystrophy

Comment

C F Inglehearn. Am J Hum Genet. 1998 Sep.

. 1998 Sep;63(3):900-1.

doi: 10.1086/301995.

No abstract available

Comment on

Localization of a novel X-linked progressive cone dystrophy gene to Xq27: evidence for genetic heterogeneity.
Bergen AA, Pinckers AJ. Bergen AA, et al. Am J Hum Genet. 1997 Jun;60(6):1468-73. doi: 10.1086/515458. Am J Hum Genet. 1997. PMID: 9199568 Free PMC article.

Localization of a novel X-linked progressive cone dystrophy gene to Xq27: evidence for genetic heterogeneity.
Bergen AA, Pinckers AJ. Bergen AA, et al. Am J Hum Genet. 1997 Jun;60(6):1468-73. doi: 10.1086/515458. Am J Hum Genet. 1997. PMID: 9199568 Free PMC article.
A gene for autosomal dominant progressive cone dystrophy (CORD5) maps to chromosome 17p12-p13.
Balciuniene J, Johansson K, Sandgren O, Wachtmeister L, Holmgren G, Forsman K. Balciuniene J, et al. Genomics. 1995 Nov 20;30(2):281-6. doi: 10.1006/geno.1995.9876. Genomics. 1995. PMID: 8586428
Meiotic drive at the myotonic dystrophy and the cone-rod dystrophy loci on chromosome 19q13.3.
Inglehearn CF, Gregory CY. Inglehearn CF, et al. Am J Hum Genet. 1997 Jun;60(6):1562-3. doi: 10.1016/S0002-9297(07)64255-4. Am J Hum Genet. 1997. PMID: 9199584 Free PMC article. No abstract available.
Multipoint linkage mapping of the Emery-Dreifuss muscular dystrophy gene.
Kress W, Müller E, Kausch K, Kullmann F, Mostacciuolo ML, Rietschel M, Rotthauwe HW, Schmalenberger B, Siciliano G, Voit T, et al. Kress W, et al. Neuromuscul Disord. 1992;2(2):111-5. doi: 10.1016/0960-8966(92)90042-5. Neuromuscul Disord. 1992. PMID: 1422197 Review.
On the genetic length of the short arm of the human X chromosome.
Ropers HH, Wieacker P, Wienker TF, Davies K, Williamson R. Ropers HH, et al. Hum Genet. 1983;65(1):53-5. doi: 10.1007/BF00285028. Hum Genet. 1983. PMID: 6315564 Review.