Smeets D - Search Results

1

No imprinting involved in the expression of DM-kinase mRNAs in mouse and human tissues.

Jansen G, Bartolomei M, Kalscheuer V, Merkx G, Wormskamp N, Mariman E, Smeets D, Ropers HH, Wieringa B. Jansen G, et al. Among authors: smeets d. Hum Mol Genet. 1993 Aug;2(8):1221-7. doi: 10.1093/hmg/2.8.1221. Hum Mol Genet. 1993. PMID: 8401505

2

Neither age nor sex influence the expression of folate sensitive common fragile sites on human chromosomes.

Smeets DF, Merkx G. Smeets DF, et al. Hum Genet. 1990 Nov;86(1):76-8. doi: 10.1007/BF00205178. Hum Genet. 1990. PMID: 2253942

3

Frequent occurrence of translocations of the short arm of chromosome 15 to other D-group chromosomes.

Smeets DF, Merkx GF, Hopman AH. Smeets DF, et al. Hum Genet. 1991 May;87(1):45-8. doi: 10.1007/BF01213090. Hum Genet. 1991. PMID: 2037282

4

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: smeets d. Hum Genet. 1987 Mar;75(3):291-3. doi: 10.1007/BF00281077. Hum Genet. 1987. PMID: 2881880

5

Evidence for specificity of the DA/DAPI technique.

Merkx GF, Hopman AH, Akkermans-Scholten AC, Smeets DF. Merkx GF, et al. Among authors: smeets df. Cytogenet Cell Genet. 1990;54(1-2):62-4. doi: 10.1159/000132957. Cytogenet Cell Genet. 1990. PMID: 1701116 No abstract available.

6

Chromosome 15p marker D15Z1 frequently maps to the short arm of other D-group chromosomes.

Smeets DF, Merkx GF, Hopman AH. Smeets DF, et al. Hum Genet. 1992 Jan;88(3):365. doi: 10.1007/BF00197282. Hum Genet. 1992. PMID: 1733845 No abstract available.

7

ICF syndrome: a new case and review of the literature.

Smeets DF, Moog U, Weemaes CM, Vaes-Peeters G, Merkx GF, Niehof JP, Hamers G. Smeets DF, et al. Hum Genet. 1994 Sep;94(3):240-6. doi: 10.1007/BF00208277. Hum Genet. 1994. PMID: 8076938 Review.

8

CDK19 is disrupted in a female patient with bilateral congenital retinal folds, microcephaly and mild mental retardation.

Mukhopadhyay A, Kramer JM, Merkx G, Lugtenberg D, Smeets DF, Oortveld MA, Blokland EA, Agrawal J, Schenck A, van Bokhoven H, Huys E, Schoenmakers EF, van Kessel AG, van Nouhuys CE, Cremers FP. Mukhopadhyay A, et al. Among authors: smeets df. Hum Genet. 2010 Sep;128(3):281-91. doi: 10.1007/s00439-010-0848-x. Epub 2010 Jun 22. Hum Genet. 2010. PMID: 20563892 Free PMC article.

9

High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridization.

Veltman JA, Schoenmakers EF, Eussen BH, Janssen I, Merkx G, van Cleef B, van Ravenswaaij CM, Brunner HG, Smeets D, van Kessel AG. Veltman JA, et al. Among authors: smeets d. Am J Hum Genet. 2002 May;70(5):1269-76. doi: 10.1086/340426. Epub 2002 Apr 9. Am J Hum Genet. 2002. PMID: 11951177 Free PMC article.

10

Identification of an unbalanced cryptic translocation between the chromosomes 8 and 13 in two sisters with mild mental retardation accompanied by mild dysmorphic features.

Kleefstra T, van de Zande G, Merkx G, Mieloo H, Hoovers JM, Smeets D. Kleefstra T, et al. Among authors: smeets d. Eur J Hum Genet. 2000 Aug;8(8):637-40. doi: 10.1038/sj.ejhg.5200500. Eur J Hum Genet. 2000. PMID: 10951526

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