Sikkema-Raddatz B - Search Results

1

Four years' cytogenetic experience with the culture of chorionic villi.

Sikkema-Raddatz B, Bouman K, Verschuuren-Bemelmans CC, Stoepker M, Mantingh A, Beekhuis JR, de Jong B. Sikkema-Raddatz B, et al. Prenat Diagn. 2000 Dec;20(12):950-5. Prenat Diagn. 2000. PMID: 11113906

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

46,XY,dup(10q) in direct CVS preparation and mosaic 48,XXXY,dup(10q) in CVS long-term culture and fetal tissue.

Sijmons RH, Sikkema-Raddatz B, Kloosterman MD, Briet JW, De Jong B, Leschot NJ. Sijmons RH, et al. Prenat Diagn. 1995 Mar;15(3):285-90. doi: 10.1002/pd.1970150314. Prenat Diagn. 1995. PMID: 7784389

4

Placental mosaicism is associated with unexplained second-trimester elevation of MShCG levels, but not with elevation of MSAFP levels.

Morssink LP, Sikkema-Raddatz B, Beekhuis JR, De Wolf BT, Mantingh A. Morssink LP, et al. Prenat Diagn. 1996 Sep;16(9):845-51. doi: 10.1002/(SICI)1097-0223(199609)16:9<845::AID-PD958>3.0.CO;2-0. Prenat Diagn. 1996. PMID: 8905899

5

The significance of placental pathology in pregnancies with unexplained abnormal concentrations of MSAFP or MShCG.

Morssink LP, de Wolf BT, Kornman LH, Beekhuis JR, van der Hall TP, Sikkema-Raddatz B, Mantingh A. Morssink LP, et al. Early Hum Dev. 1996 Dec 30;47 Suppl:S63-5. doi: 10.1016/s0378-3782(96)01823-3. Early Hum Dev. 1996. PMID: 9031844 No abstract available.

6

Probability tables for exclusion of mosaicism in prenatal diagnosis.

Sikkema-Raddatz B, Castedo S, Te Meerman GJ. Sikkema-Raddatz B, et al. Prenat Diagn. 1997 Feb;17(2):115-8. doi: 10.1002/(sici)1097-0223(199702)17:2<115::aid-pd37>3.0.co;2-a. Prenat Diagn. 1997. PMID: 9061758

7

A 46,XX,der(13;14)(q10;q10),+21 child born after a 45,XX,der(13;14)(q10;q10) chromosomal finding in CVS.

Sikkema-Raddatz B, Verschuuren-Bemelmans CC, Kloosterman M, de Jong B. Sikkema-Raddatz B, et al. Prenat Diagn. 1997 Nov;17(11):1086-8. doi: 10.1002/(sici)1097-0223(199711)17:11<1086::aid-pd162>3.0.co;2-i. Prenat Diagn. 1997. PMID: 9399361 No abstract available.

8

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.

9

Trisomy 12 mosaicism in CVS culture confirmed in the fetus.

Sikkema-Raddatz B, Bouman K, Verschuuren-Bemelmans CC, de Jong B. Sikkema-Raddatz B, et al. Prenat Diagn. 1999 Dec;19(12):1176-7. Prenat Diagn. 1999. PMID: 10590440 No abstract available.

10

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

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