Brunner H - Search Results

1

Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophy.

Ashizawa T, Anvret M, Baiget M, Barceló JM, Brunner H, Cobo AM, Dallapiccola B, Fenwick RG Jr, Grandell U, Harley H, et al. Ashizawa T, et al. Among authors: brunner h. Am J Hum Genet. 1994 Mar;54(3):414-23. Am J Hum Genet. 1994. PMID: 8116611 Free PMC article.

2

Presymptomatic diagnosis of myotonic dystrophy.

Brunner HG, Nillesen W, van Oost BA, Jansen G, Wieringa B, Ropers HH, Smeets HJ. Brunner HG, et al. J Med Genet. 1992 Nov;29(11):780-4. doi: 10.1136/jmg.29.11.780. J Med Genet. 1992. PMID: 1453426 Free PMC article.

3

Use of variable simple sequence motifs as genetic markers: application to study of myotonic dystrophy.

Smeets HJ, Brunner HG, Ropers HH, Wieringa B. Smeets HJ, et al. Among authors: brunner hg. Hum Genet. 1989 Oct;83(3):245-51. doi: 10.1007/BF00285165. Hum Genet. 1989. PMID: 2571562

4

Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM).

Brunner HG, Korneluk RG, Coerwinkel-Driessen M, MacKenzie A, Smeets H, Lambermon HM, van Oost BA, Wieringa B, Ropers HH. Brunner HG, et al. Hum Genet. 1989 Mar;81(4):308-10. doi: 10.1007/BF00283680. Hum Genet. 1989. PMID: 2703233

5

Three-point linkage analysis employing C3 and 19cen markers assigns the myotonic dystrophy gene to 19q.

Friedrich U, Brunner H, Smeets D, Lambermon E, Ropers HH. Friedrich U, et al. Among authors: brunner h. Hum Genet. 1987 Mar;75(3):291-3. doi: 10.1007/BF00281077. Hum Genet. 1987. PMID: 2881880

6

Tight linkage between myotonic dystrophy and apolipoprotein E genes revealed with allele-specific oligonucleotides.

Smeets B, Poddighe J, Brunner H, Ropers HH, Wieringa B. Smeets B, et al. Among authors: brunner h. Hum Genet. 1988 Sep;80(1):49-52. doi: 10.1007/BF00451455. Hum Genet. 1988. PMID: 3417303

7

Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm.

Jansen G, Willems P, Coerwinkel M, Nillesen W, Smeets H, Vits L, Höweler C, Brunner H, Wieringa B. Jansen G, et al. Among authors: brunner h. Am J Hum Genet. 1994 Apr;54(4):575-85. Am J Hum Genet. 1994. PMID: 8128954 Free PMC article.

8

Influence of sex of the transmitting parent as well as of parental allele size on the CTG expansion in myotonic dystrophy (DM).

Brunner HG, Brüggenwirth HT, Nillesen W, Jansen G, Hamel BC, Hoppe RL, de Die CE, Höweler CJ, van Oost BA, Wieringa B, et al. Brunner HG, et al. Am J Hum Genet. 1993 Nov;53(5):1016-23. Am J Hum Genet. 1993. PMID: 8213829 Free PMC article.

9

Dinucleotide repeat polymorphism at locus D19S207, close to the myotonic dystrophy (DM) gene.

Jansen G, Coerwinkel-Driessen M, Nillesen W, Brunner H, Wieringa B. Jansen G, et al. Among authors: brunner h. Hum Mol Genet. 1993 Mar;2(3):333. doi: 10.1093/hmg/2.3.333. Hum Mol Genet. 1993. PMID: 8499928 No abstract available.

10

Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13.

Gong Y, Vikkula M, Boon L, Liu J, Beighton P, Ramesar R, Peltonen L, Somer H, Hirose T, Dallapiccola B, De Paepe A, Swoboda W, Zabel B, Superti-Furga A, Steinmann B, Brunner HG, Jans A, Boles RG, Adkins W, van den Boogaard MJ, Olsen BR, Warman ML. Gong Y, et al. Among authors: brunner hg. Am J Hum Genet. 1996 Jul;59(1):146-51. Am J Hum Genet. 1996. PMID: 8659519 Free PMC article.

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