Pearson PL - Search Results

1

Two step procedure for early diagnosis of polycystic kidney disease with polymorphic DNA markers on both sides of the gene.

Breuning MH, Snijdewint FG, Dauwerse JG, Saris JJ, Bakker E, Pearson PL, vanOmmen GJ. Breuning MH, et al. Among authors: pearson pl. J Med Genet. 1990 Oct;27(10):614-7. doi: 10.1136/jmg.27.10.614. J Med Genet. 1990. PMID: 1978861 Free PMC article.

2

Presymptomatic, prenatal, and exclusion testing for Huntington disease using seven closely linked DNA markers.

Skraastad MI, Verwest A, Bakker E, Vegter-van der Vlis M, van Leeuwen-Cornelisse I, Roos RA, Pearson PL, van Ommen GJ. Skraastad MI, et al. Among authors: pearson pl. Am J Med Genet. 1991 May 1;39(2):217-22. doi: 10.1002/ajmg.1320390221. Am J Med Genet. 1991. PMID: 1829584

3

Rapid detection of chromosome 16 inversion in acute nonlymphocytic leukemia, subtype M4: regional localization of the breakpoint in 16p.

Dauwerse JG, Kievits T, Beverstock GC, van der Keur D, Smit E, Wessels HW, Hagemeijer A, Pearson PL, van Ommen GJ, Breuning MH. Dauwerse JG, et al. Among authors: pearson pl. Cytogenet Cell Genet. 1990;53(2-3):126-8. doi: 10.1159/000132911. Cytogenet Cell Genet. 1990. PMID: 2369839

4

Mapping of recombinants near the Huntington disease locus by using G8 (D4S10) and newly isolated markers in the D4S10 region.

Skraastad MI, Bakker E, de Lange LF, Vegter-van der Vlis M, Klein-Breteler EG, van Ommen GJ, Pearson PL. Skraastad MI, et al. Among authors: pearson pl. Am J Hum Genet. 1989 Apr;44(4):560-6. Am J Hum Genet. 1989. PMID: 2564732 Free PMC article.

5

Characterization of new probes for diagnosis of polycystic kidney disease (PKD1).

Breuning MH, Verwest A, Ijdo J, Saris JJ, Keith T, Reeders ST, van Ommen GJ, Pearson PL. Breuning MH, et al. Among authors: pearson pl. Prog Clin Biol Res. 1989;305:69-75. Prog Clin Biol Res. 1989. PMID: 2569743 No abstract available.

6

Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.

Den Dunnen JT, Grootscholten PM, Bakker E, Blonden LA, Ginjaar HB, Wapenaar MC, van Paassen HM, van Broeckhoven C, Pearson PL, van Ommen GJ. Den Dunnen JT, et al. Among authors: pearson pl. Am J Hum Genet. 1989 Dec;45(6):835-47. Am J Hum Genet. 1989. PMID: 2573997 Free PMC article.

7

Long-range mapping in the research and diagnosis of genetic disease.

van Ommen GJ, Pearson PL. van Ommen GJ, et al. Among authors: pearson pl. Genome. 1989;31(2):730-6. doi: 10.1139/g89-131. Genome. 1989. PMID: 2576651 Review.

8

Germinal mosaicism increases the recurrence risk for 'new' Duchenne muscular dystrophy mutations.

Bakker E, Veenema H, Den Dunnen JT, van Broeckhoven C, Grootscholten PM, Bonten EJ, van Ommen GJ, Pearson PL. Bakker E, et al. Among authors: pearson pl. J Med Genet. 1989 Sep;26(9):553-9. doi: 10.1136/jmg.26.9.553. J Med Genet. 1989. PMID: 2810338 Free PMC article.

9

DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.

Bakker E, Bonten EJ, De Lange LF, Veenema H, Majoor-Krakauer D, Hofker MH, Van Ommen GJ, Pearson PL. Bakker E, et al. Among authors: pearson pl. J Med Genet. 1986 Dec;23(6):573-80. doi: 10.1136/jmg.23.6.573. J Med Genet. 1986. PMID: 2879929 Free PMC article.

10

Improved early diagnosis of adult polycystic kidney disease with flanking DNA markers.

Breuning MH, Reeders ST, Brunner H, Ijdo JW, Saris JJ, Verwest A, van Ommen GJ, Pearson PL. Breuning MH, et al. Among authors: pearson pl. Lancet. 1987 Dec 12;2(8572):1359-61. doi: 10.1016/s0140-6736(87)91256-6. Lancet. 1987. PMID: 2890952

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