Smeets DF - Search Results

1

Prospective screening for subtelomeric rearrangements in children with mental retardation of unknown aetiology: the Amsterdam experience.

van Karnebeek CD, Koevoets C, Sluijter S, Bijlsma EK, Smeets DF, Redeker EJ, Hennekam RC, Hoovers JM. van Karnebeek CD, et al. Among authors: smeets df. J Med Genet. 2002 Aug;39(8):546-53. doi: 10.1136/jmg.39.8.546. J Med Genet. 2002. PMID: 12161591 Free PMC article.

2

No justification of routine screening for 22q11 deletions in patients with overt cleft palate.

Ruiter EM, Bongers EM, Smeets D, Kuijpers-Jagtman AM, Hamel BC. Ruiter EM, et al. Clin Genet. 2003 Sep;64(3):216-9. doi: 10.1034/j.1399-0004.2003.00134.x. Clin Genet. 2003. PMID: 12919136

3

Another patient with a deletion 14q11.2q13.

Govaerts L, Toorman J, Blij-Philipsen MV, Smeets D. Govaerts L, et al. Ann Genet. 1996;39(4):197-200. Ann Genet. 1996. PMID: 9037346

4

A novel duplication of chromosome (13)(q14.1q21.3) in a patient with mental retardation and microcephaly.

Verhoeven W, Ruiter M, Egger J, Tuinier S, Smeets D. Verhoeven W, et al. Genet Couns. 2009;20(1):45-51. Genet Couns. 2009. PMID: 19400541

5

Interphase cytogenetics of hematological cancer: comparison of classical karyotyping and in situ hybridization using a panel of eleven chromosome specific DNA probes.

Poddighe PJ, Moesker O, Smeets D, Awwad BH, Ramaekers FC, Hopman AH. Poddighe PJ, et al. Cancer Res. 1991 Apr 1;51(7):1959-67. Cancer Res. 1991. PMID: 2004382

6

Low level of mosaicism for a balanced translocation as a case of unbalanced offspring.

Smeets DF. Smeets DF. Am J Med Genet. 1993 Jan 1;45(1):114-5. doi: 10.1002/ajmg.1320450129. Am J Med Genet. 1993. PMID: 8418644 No abstract available.

7

Preaxial polydactyly in the 4p- syndrome.

Schrander-Stumpel CT, Rijnvos WP, van der Blij-Philipsen M, Drogtrop A, Smeets D, Fryns JP. Schrander-Stumpel CT, et al. Genet Couns. 1998;9(1):63-5. Genet Couns. 1998. PMID: 9555593 No abstract available.

8

Changes in yearly birth prevalence rates of children with Down syndrome in the period 1986-2007 in The Netherlands.

de Graaf G, Haveman M, Hochstenbach R, Engelen J, Gerssen-Schoorl K, Poddighe P, Smeets D, van Hove G. de Graaf G, et al. J Intellect Disabil Res. 2011 May;55(5):462-73. doi: 10.1111/j.1365-2788.2011.01398.x. Epub 2011 Mar 6. J Intellect Disabil Res. 2011. PMID: 21375641

9

Anesthesiologic problems in Williams syndrome: the CACNL2A locus is not involved.

Mammi I, Iles DE, Smeets D, Clementi M, Tenconi R. Mammi I, et al. Hum Genet. 1996 Sep;98(3):317-20. doi: 10.1007/s004390050214. Hum Genet. 1996. PMID: 8707301 Free article.

10

Prenatal cell-free DNA testing of women with pregnancy-associated cancer: a retrospective cross-sectional study.

Heesterbeek CJ, Tjan-Heijnen VCG, Heimovaara JH, Lenaerts L, Lok C, Vriens IJH, Van Opstal D, Boon EMJ, Sie D, de Die-Smulders CEM, Amant F, Macville MVE; Dutch NIPT Consortium. Heesterbeek CJ, et al. Lancet Reg Health Eur. 2024 Aug 7;45:101024. doi: 10.1016/j.lanepe.2024.101024. eCollection 2024 Oct. Lancet Reg Health Eur. 2024. PMID: 39220433 Free PMC article.

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