Kivlin J - Search Results

1

The genetic aspects of neurofibromatosis.

Carey JC, Baty BJ, Johnson JP, Morrison T, Skolnick M, Kivlin J. Carey JC, et al. Among authors: kivlin j. Ann N Y Acad Sci. 1986;486:45-56. doi: 10.1111/j.1749-6632.1986.tb48061.x. Ann N Y Acad Sci. 1986. PMID: 3105404

2

Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17.

Barker D, Wright E, Nguyen K, Cannon L, Fain P, Goldgar D, Bishop DT, Carey J, Baty B, Kivlin J, et al. Barker D, et al. Among authors: kivlin j. Science. 1987 May 29;236(4805):1100-2. doi: 10.1126/science.3107130. Science. 1987. PMID: 3107130

3

A genomic search for linkage of neurofibromatosis to RFLPs.

Barker D, Wright E, Nguyen K, Cannon L, Fain P, Goldgar D, Bishop DT, Carey J, Kivlin J, Willard H, et al. Barker D, et al. Among authors: kivlin j. J Med Genet. 1987 Sep;24(9):536-8. doi: 10.1136/jmg.24.9.536. J Med Genet. 1987. PMID: 2889831 Free PMC article.

4

Linkage analysis of Von Recklinghausen neurofibromatosis: chromosomes 4 and 19.

Dietz JN, Robbins T, Cannon LA, Schwartz CE, Carey JC, Johnson JP, Kivlin J, Skolnick MH. Dietz JN, et al. Among authors: kivlin j. Genet Epidemiol. 1986;3(5):313-21. doi: 10.1002/gepi.1370030504. Genet Epidemiol. 1986. PMID: 3096816

5

Genetic analysis of NF1: identification of close flanking markers on chromosome 17.

Fain PR, Barker DF, Goldgar DE, Wright E, Nguyen K, Carey J, Johnson J, Kivlin J, Willard H, Mathew C, et al. Fain PR, et al. Among authors: kivlin j. Genomics. 1987 Dec;1(4):340-5. doi: 10.1016/0888-7543(87)90034-6. Genomics. 1987. PMID: 3130304

6

Brachymesomelic dysplasia with Peters anomaly of the eye results from disruptions of the X chromosome near the SHOX and SOX3 genes.

Bleyl SB, Byrne JL, South ST, Dries DC, Stevenson DA, Rope AF, Vianna-Morgante AM, Schoenwolf GC, Kivlin JD, Brothman A, Carey JC. Bleyl SB, et al. Among authors: kivlin jd. Am J Med Genet A. 2007 Dec 1;143A(23):2785-95. doi: 10.1002/ajmg.a.32036. Am J Med Genet A. 2007. PMID: 17994562

7

Linkage analysis in lattice corneal dystrophy.

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

8

Brachymesomelia and Peters anomaly: a new syndrome.

Kivlin JD, Carey JC, Richey MA. Kivlin JD, et al. Am J Med Genet. 1993 Feb 15;45(4):416-9. doi: 10.1002/ajmg.1320450403. Am J Med Genet. 1993. PMID: 8465841

9

Linkage analysis in dominant optic atrophy.

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

10

A progressive early onset cataract gene maps to human chromosome 17q24.

Armitage MM, Kivlin JD, Ferrell RE. Armitage MM, et al. Among authors: kivlin jd. Nat Genet. 1995 Jan;9(1):37-40. doi: 10.1038/ng0195-37. Nat Genet. 1995. PMID: 7704021

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