Pearson P - Search Results

1

Menkes kinky hair disease: a search for closely linked restriction fragment length polymorphism.

Wieacker P, Horn N, Pearson P, Wienker TF, McKay E, Ropers HH. Wieacker P, et al. Among authors: pearson p. Hum Genet. 1983;64(2):139-42. doi: 10.1007/BF00327110. Hum Genet. 1983. PMID: 6576980

2

Norrie's disease: close linkage with genetic markers from the proximal short arm of the X chromosome.

Gal A, Stolzenberger C, Wienker T, Wieacker P, Ropers HH, Friedrich U, Bleeker-Wagemakers L, Pearson P, Warburg M. Gal A, et al. Among authors: pearson p. Clin Genet. 1985 Mar;27(3):282-3. doi: 10.1111/j.1399-0004.1985.tb00221.x. Clin Genet. 1985. PMID: 3857130 No abstract available.

3

Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal Xq.

Cremers FP, van de Pol TJ, Wieringa B, Hofker MH, Pearson PL, Pfeiffer RA, Mikkelsen M, Tabor A, Ropers HH. Cremers FP, et al. Among authors: pearson pl. Am J Hum Genet. 1988 Oct;43(4):452-61. Am J Hum Genet. 1988. PMID: 3177387 Free PMC article.

4

Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids.

Wieacker P, Davies KE, Cooke HJ, Pearson PL, Williamson R, Bhattacharya S, Zimmer J, Ropers HH. Wieacker P, et al. Among authors: pearson pl. Am J Hum Genet. 1984 Mar;36(2):265-76. Am J Hum Genet. 1984. PMID: 6324578 Free PMC article.

5

Carrier detection in Duchenne muscular dystrophy by use of cloned DNA sequences.

Wieacker P, Davies K, Pearson P, Ropers HH. Wieacker P, et al. Among authors: pearson p. Lancet. 1983 Jun 11;1(8337):1325-6. doi: 10.1016/s0140-6736(83)92429-7. Lancet. 1983. PMID: 6134107 No abstract available.

6

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy.

Hofker MH, Wapenaar MC, Goor N, Bakker E, van Ommen GJ, Pearson PL. Hofker MH, et al. Among authors: pearson pl. Hum Genet. 1985;70(2):148-56. doi: 10.1007/BF00273073. Hum Genet. 1985. PMID: 2989153

7

Fine mapping of the Huntington disease linked D4S10 locus by non-radioactive in situ hybridization.

Landegent JE, Jansen in de Wal N, Fisser-Groen YM, Bakker E, van der Ploeg M, Pearson PL. Landegent JE, et al. Among authors: pearson pl. Hum Genet. 1986 Aug;73(4):354-7. doi: 10.1007/BF00279100. Hum Genet. 1986. PMID: 2943662

8

Multipoint linkage analysis of the short arm of the human X chromosome in families with X-linked muscular dystrophy.

Wilcox DE, Affara NA, Yates JR, Ferguson-Smith MA, Pearson PL. Wilcox DE, et al. Among authors: pearson pl. Hum Genet. 1985;70(4):365-75. doi: 10.1007/BF00295379. Hum Genet. 1985. PMID: 3860471

9

Genetic linkage relationships of seven DNA probes with Duchenne and Becker muscular dystrophy.

Brown CS, Thomas NS, Sarfarazi M, Davies KE, Kunkel L, Pearson PL, Kingston HM, Shaw DJ, Harper PS. Brown CS, et al. Among authors: pearson pl. Hum Genet. 1985;71(1):62-74. doi: 10.1007/BF00295671. Hum Genet. 1985. PMID: 2993158

10

Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families.

Arveiler B, Oberlé I, Vincent A, Hofker MH, Pearson PL, Mandel JL. Arveiler B, et al. Among authors: pearson pl. Am J Hum Genet. 1988 Feb;42(2):380-9. Am J Hum Genet. 1988. PMID: 2893549 Free PMC article.

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