Sikkema-Raddatz B - Search Results

1

FISH and array-CGH analysis of a complex chromosome 3 aberration suggests that loss of CNTN4 and CRBN contributes to mental retardation in 3pter deletions.

Dijkhuizen T, van Essen T, van der Vlies P, Verheij JB, Sikkema-Raddatz B, van der Veen AY, Gerssen-Schoorl KB, Buys CH, Kok K. Dijkhuizen T, et al. Am J Med Genet A. 2006 Nov 15;140(22):2482-7. doi: 10.1002/ajmg.a.31487. Am J Med Genet A. 2006. PMID: 17036314

2

Prenatal diagnosis in two cases of de novo complex balanced chromosomal rearrangements. Three-year follow-up in one case.

Sikkema-Raddatz B, Sijmons RH, Tan-Sindhunata MB, van der Veen AY, Brunsting R, de Vries B, Beekhuis JR, Bekedam DJ, van Aken B, de Jong B. Sikkema-Raddatz B, et al. Prenat Diagn. 1995 May;15(5):467-73. doi: 10.1002/pd.1970150510. Prenat Diagn. 1995. PMID: 7644437

3

Three cases of mosaicism for balanced reciprocal translocations.

Leegte B, Sikkema-Raddatz B, Hordijk R, Bouman K, van Essen T, Castedo S, de Jong B. Leegte B, et al. Am J Med Genet. 1998 Oct 12;79(5):362-5. Am J Med Genet. 1998. PMID: 9779802 Review.

4

Two unbalanced segregation products due to a maternal t(7;16)inv(16).

Leegte B, Sikkema-Raddatz B, Hordijk R, Davelaar I, van der Veen A, Cobben JM. Leegte B, et al. Prenat Diagn. 2001 Jul;21(7):550-2. doi: 10.1002/pd.107. Prenat Diagn. 2001. PMID: 11494289

5

Application of a comprehensive subtelomere array in clinical diagnosis of mental retardation.

Kok K, Dijkhuizen T, Swart YE, Zorgdrager H, van der Vlies P, Fehrmann R, te Meerman GJ, Gerssen-Schoorl KB, van Essen T, Sikkema-Raddatz B, Buys CH. Kok K, et al. Eur J Med Genet. 2005 Jul-Sep;48(3):250-62. doi: 10.1016/j.ejmg.2005.04.007. Eur J Med Genet. 2005. PMID: 16179221

6

BCL6 alternative breakpoint region break and homozygous deletion of 17q24 in the nodular lymphocyte predominance type of Hodgkin's lymphoma-derived cell line DEV.

Atayar C, Kok K, Kluiver J, Bosga A, van den Berg E, van der Vlies P, Blokzijl T, Harms G, Davelaar I, Sikkema-Raddatz B, Martin-Subero JI, Siebert R, Poppema S, van den Berg A. Atayar C, et al. Hum Pathol. 2006 Jun;37(6):675-83. doi: 10.1016/j.humpath.2006.01.018. Hum Pathol. 2006. PMID: 16733207

7

Quality aspects of prenatal cytogenetic diagnosis: determining the effect of various factors involved in handling amniotic fluid and chorionic villus material for cytogenetic diagnosis.

Sikkema-Raddatz B, Suijkerbuijk R, Bouman K, de Jong B, Buys CH, te Meerman GJ. Sikkema-Raddatz B, et al. Prenat Diagn. 2006 Sep;26(9):791-800. doi: 10.1002/pd.1505. Prenat Diagn. 2006. PMID: 16821245

8

An absolute procedure to test the growth potential of medium and the influence of decreased oxygen tension in primary amniotic fluid cell cultures.

Sikkema-Raddatz B, Suijkerbuijk R, van der Vlag J, Stoepker M, Buys CH, te Meerman GJ. Sikkema-Raddatz B, et al. Prenat Diagn. 2006 Sep;26(9):855-60. doi: 10.1002/pd.1522. Prenat Diagn. 2006. PMID: 16821249

9

Mosaic isodicentric chromosome 18q: sixth report and review.

Oudesluijs GG, Hulzebos CV, Sikkema-Raddatz B, Van Essen AJ. Oudesluijs GG, et al. Genet Couns. 2006;17(4):395-400. Genet Couns. 2006. PMID: 17375524

10

In vitro fertilization with preimplantation genetic screening.

Mastenbroek S, Twisk M, van Echten-Arends J, Sikkema-Raddatz B, Korevaar JC, Verhoeve HR, Vogel NE, Arts EG, de Vries JW, Bossuyt PM, Buys CH, Heineman MJ, Repping S, van der Veen F. Mastenbroek S, et al. N Engl J Med. 2007 Jul 5;357(1):9-17. doi: 10.1056/NEJMoa067744. Epub 2007 Jul 4. N Engl J Med. 2007. PMID: 17611204 Free article. Clinical Trial.

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