Ploughman LM - Search Results

1

A new test for linkage in the presence of locus heterogeneity.

MacLean CJ, Ploughman LM, Diehl SR, Kendler KS. MacLean CJ, et al. Among authors: ploughman lm. Am J Hum Genet. 1992 Jun;50(6):1259-66. Am J Hum Genet. 1992. PMID: 1598905 Free PMC article.

2

Major-locus contributions to variability of the craniofacial feature dystopia canthorum in Waardenburg syndrome.

Reynolds JE, Marazita ML, Meyer JM, Stevens CA, Eaves LJ, Arnos KS, Ploughman LM, MacLean C, Nance WE, Diehl SR. Reynolds JE, et al. Among authors: ploughman lm. Am J Hum Genet. 1996 Feb;58(2):384-92. Am J Hum Genet. 1996. PMID: 8571965 Free PMC article.

3

A refined genetic map of the region of chromosome 17 surrounding the von Recklinghausen neurofibromatosis (NF1) gene.

Diehl SR, Boehnke M, Erickson RP, Ploughman LM, Seiler KA, Lieberman JL, Clarke HB, Bruce MA, Schorry EK, Pericak-Vance M, et al. Diehl SR, et al. Among authors: ploughman lm. Am J Hum Genet. 1989 Jan;44(1):33-7. Am J Hum Genet. 1989. PMID: 2491779 Free PMC article.

4

Linkage analysis of peripheral neurofibromatosis to DNA markers on chromosome 8.

Diehl SR, Boehnke M, Collins FS, Erickson RP, Karolyi IJ, Ploughman LM, Pericak-Vance MA, Aylsworth AS, Roses AD. Diehl SR, et al. Among authors: ploughman lm. J Med Genet. 1987 Sep;24(9):532-4. doi: 10.1136/jmg.24.9.532. J Med Genet. 1987. PMID: 3118034 Free PMC article.

5

Linkage analysis of von Recklinghausen neurofibromatosis to DNA markers on chromosome 17.

Diehl SR, Boehnke M, Erickson RP, Baxter AB, Bruce MA, Lieberman JL, Platt DJ, Ploughman LM, Seiler KA, Sweet AM, et al. Diehl SR, et al. Among authors: ploughman lm. Genomics. 1987 Dec;1(4):361-3. doi: 10.1016/0888-7543(87)90039-5. Genomics. 1987. PMID: 2896631 Free article.

6

Analysis of locus heterogeneity in Waardenburg syndrome types 1 and 2 using highly informative microsatellite markers.

Reynolds JE, Arnos KS, Landa B, Stevens CA, Salbert BA, Wright L, Duke B, Hunt W, Marazita ML, Ploughman L, et al. Reynolds JE, et al. Hum Hered. 1995 Sep-Oct;45(5):243-52. doi: 10.1159/000154307. Hum Hered. 1995. PMID: 7590754

7

Estimating the power of a proposed linkage study for a complex genetic trait.

Ploughman LM, Boehnke M. Ploughman LM, et al. Am J Hum Genet. 1989 Apr;44(4):543-51. Am J Hum Genet. 1989. PMID: 2929597 Free PMC article.

8

Heterogeneity testing for Alzheimer's disease within and between data sets.

Miller LL, Ploughman LM, Marazita ML. Miller LL, et al. Among authors: ploughman lm. Genet Epidemiol. 1993;10(6):443-7. doi: 10.1002/gepi.1370100619. Genet Epidemiol. 1993. PMID: 8314041

9

Genetic epidemiological studies of early-onset deafness in the U.S. school-age population.

Marazita ML, Ploughman LM, Rawlings B, Remington E, Arnos KS, Nance WE. Marazita ML, et al. Among authors: ploughman lm. Am J Med Genet. 1993 Jun 15;46(5):486-91. doi: 10.1002/ajmg.1320460504. Am J Med Genet. 1993. PMID: 8322805

10

Asp92Asn polymorphism in the myeloid IgA Fc receptor is associated with myocardial infarction in two disparate populations: CARE and WOSCOPS.

Iakoubova OA, Tong CH, Chokkalingam AP, Rowland CM, Kirchgessner TG, Louie JZ, Ploughman LM, Sabatine MS, Campos H, Catanese JJ, Leong DU, Young BA, Lew D, Tsuchihashi Z, Luke MM, Packard CJ, Zerba KE, Shaw PM, Shepherd J, Devlin JJ, Sacks FM. Iakoubova OA, et al. Among authors: ploughman lm. Arterioscler Thromb Vasc Biol. 2006 Dec;26(12):2763-8. doi: 10.1161/01.ATV.0000247248.76409.8b. Epub 2006 Sep 28. Arterioscler Thromb Vasc Biol. 2006. PMID: 17008591

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

11 results

Search Page

Filters