Hofker MH - Search Results

1

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: hofker mh. Am J Hum Genet. 1988 Oct;43(4):452-61. Am J Hum Genet. 1988. PMID: 3177387 Free PMC article.

2

An interstitial duplication of the X chromosome in a male allows physical fine mapping of probes from the Xq13-q22 region.

Cremers FP, Pfeiffer RA, van de Pol TJ, Hofker MH, Kruse TA, Wieringa B, Ropers HH. Cremers FP, et al. Among authors: hofker mh. Hum Genet. 1987 Sep;77(1):23-7. doi: 10.1007/BF00284707. Hum Genet. 1987. PMID: 3476455

3

Development of additional RFLP probes near the locus for Duchenne muscular dystrophy by cosmid cloning of the DXS84 (754) locus.

Hofker MH, van Ommen GJ, Bakker E, Burmeister M, Pearson PL. Hofker MH, et al. Hum Genet. 1986 Nov;74(3):270-4. doi: 10.1007/BF00282547. Hum Genet. 1986. PMID: 2877935

4

Isolation of a random cosmid clone, cX5, which defines a new polymorphic locus DXS148 near the locus for Duchenne muscular dystrophy.

Hofker MH, Bergen AA, Skraastad MI, Bakker E, Francke U, Wieringa B, Bartley J, van Ommen GJ, Pearson PL. Hofker MH, et al. Hum Genet. 1986 Nov;74(3):275-9. doi: 10.1007/BF00282548. Hum Genet. 1986. PMID: 2877936

5

Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardation.

Hofker MH, Bergen AA, Skraastad MI, Carpenter NJ, Veenema H, Connor JM, Bakker E, van Ommen GJ, Pearson PL. Hofker MH, et al. Am J Hum Genet. 1987 Apr;40(4):312-28. Am J Hum Genet. 1987. PMID: 2883888 Free PMC article.

6

A new DNA probe proximal to and closely linked to fragile X.

Carpenter NJ, Veenema H, Bakker E, Hofker MH, Pearson PL. Carpenter NJ, et al. Among authors: hofker mh. Am J Med Genet. 1987 Jul;27(3):731-2. doi: 10.1002/ajmg.1320270332. Am J Med Genet. 1987. PMID: 2888310 No abstract available.

7

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: hofker mh. Am J Hum Genet. 1988 Feb;42(2):380-9. Am J Hum Genet. 1988. PMID: 2893549 Free PMC article.

8

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. Hum Genet. 1985;70(2):148-56. doi: 10.1007/BF00273073. Hum Genet. 1985. PMID: 2989153

9

Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.

Francke U, Ochs HD, de Martinville B, Giacalone J, Lindgren V, Distèche C, Pagon RA, Hofker MH, van Ommen GJ, Pearson PL, et al. Francke U, et al. Among authors: hofker mh. Am J Hum Genet. 1985 Mar;37(2):250-67. Am J Hum Genet. 1985. PMID: 4039107 Free PMC article.

10

Inactivation of Apoe and Apoc1 by two consecutive rounds of gene targeting: effects on mRNA expression levels of gene cluster members.

van Ree JH, van den Broek WJ, van der Zee A, Dahlmans VE, Wieringa B, Frants RR, Havekes LM, Hofker MH. van Ree JH, et al. Among authors: hofker mh. Hum Mol Genet. 1995 Aug;4(8):1403-9. doi: 10.1093/hmg/4.8.1403. Hum Mol Genet. 1995. PMID: 7581381 Free article.

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