Smeets HJ - Search Results

1

Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndrome.

Meijers-Heijboer EJ, Sandkuijl LA, Brunner HG, Smeets HJ, Hoogeboom AJ, Deelen WH, van Hemel JO, Nelen MR, Smeets DF, Niermeijer MF, et al. Meijers-Heijboer EJ, et al. Among authors: smeets hj, smeets df. J Med Genet. 1992 Dec;29(12):853-7. doi: 10.1136/jmg.29.12.853. J Med Genet. 1992. PMID: 1362220 Free PMC article.

2

Familial Angelman syndrome with a crossover in the critical deletion region.

Nelen MR, Van der Burgt CJ, Nillesen WN, Vis A, Smeets HJ. Nelen MR, et al. Among authors: smeets hj. Am J Med Genet. 1994 Sep 1;52(3):352-7. doi: 10.1002/ajmg.1320520320. Am J Med Genet. 1994. PMID: 7810569

3

A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19.

Brunner HG, Smeets H, Lambermon HM, Coerwinkel-Driessen M, van Oost BA, Wieringa B, Ropers HH. Brunner HG, et al. Genomics. 1989 Oct;5(3):589-95. doi: 10.1016/0888-7543(89)90027-x. Genomics. 1989. PMID: 2575588

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

Presymptomatic diagnosis of myotonic dystrophy.

Brunner HG, Nillesen W, van Oost BA, Jansen G, Wieringa B, Ropers HH, Smeets HJ. Brunner HG, et al. Among authors: smeets hj. 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.

6

Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15.

Smeets DF, Hamel BC, Nelen MR, Smeets HJ, Bollen JH, Smits AP, Ropers HH, van Oost BA. Smeets DF, et al. Among authors: smeets hj. N Engl J Med. 1992 Mar 19;326(12):807-11. doi: 10.1056/NEJM199203193261206. N Engl J Med. 1992. PMID: 1538725 Free article. No abstract available.

7

Identification of variable simple sequence motifs in 19q13.2-qter: markers for the myotonic dystrophy locus.

Smeets HJ, Hermens R, Brunner HG, Ropers HH, Wieringa B. Smeets HJ, et al. Genomics. 1991 Feb;9(2):257-63. doi: 10.1016/0888-7543(91)90250-i. Genomics. 1991. PMID: 1840564

8

Genetic linkage with chromosome 19 but not chromosome 17 in a family with myotonic dystrophy associated with hereditary motor and sensory neuropathy.

Brunner HG, Spaans F, Smeets HJ, Coerwinkel-Driessen M, Hulsebos T, Wieringa B, Ropers HH. Brunner HG, et al. Among authors: smeets hj. Neurology. 1991 Jan;41(1):80-4. doi: 10.1212/wnl.41.1.80. Neurology. 1991. PMID: 1985299

9

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. Hum Genet. 1989 Oct;83(3):245-51. doi: 10.1007/BF00285165. Hum Genet. 1989. PMID: 2571562

10

Anticipation resulting in elimination of the myotonic dystrophy gene: a follow up study of one extended family.

de Die-Smulders CE, Höweler CJ, Mirandolle JF, Brunner HG, Hovers V, Brüggenwirth H, Smeets HJ, Geraedts JP. de Die-Smulders CE, et al. Among authors: smeets hj. J Med Genet. 1994 Aug;31(8):595-601. doi: 10.1136/jmg.31.8.595. J Med Genet. 1994. PMID: 7815415 Free PMC article.

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

289 results

Search Page

Filters