Govaerts L - Search Results

1

Deletion (8)(q22) as the only chromosomal abnormality in a patient with RAEB-t with progression to acute myelocytic leukemia.

Govaerts L, Daenen S, Bong B, Breed A, de Jong B. Govaerts L, et al. Cancer Genet Cytogenet. 1988 Feb;30(2):319-21. doi: 10.1016/0165-4608(88)90201-4. Cancer Genet Cytogenet. 1988. PMID: 3422584

2

A novel case of infantile sacral teratoma and a constitutional t(12;15)(q13;q25) pat.

Veltman I, van Asseldonk M, Schepens M, Stoop H, Looijenga L, Wouters C, Govaerts L, Suijkerbuijk R, van Kessel A. Veltman I, et al. Among authors: govaerts l. Cancer Genet Cytogenet. 2002 Jul 1;136(1):17-22. doi: 10.1016/s0165-4608(01)00666-5. Cancer Genet Cytogenet. 2002. PMID: 12165446

3

Abnormal karyotype in the chorion, not confirmed in a subsequently aborted fetus.

Breed A, Mantingh A, Govaerts L, Boogert A, Anders G, Laurini R. Breed A, et al. Among authors: govaerts l. Prenat Diagn. 1986 Sep-Oct;6(5):375-7. doi: 10.1002/pd.1970060506. Prenat Diagn. 1986. PMID: 3774766

4

The tumor suppressor gene FBXW7 is disrupted by a constitutional t(3;4)(q21;q31) in a patient with renal cell cancer.

Kuiper RP, Vreede L, Venkatachalam R, Ricketts C, Kamping E, Verwiel E, Govaerts L, Debiec-Rychter M, Lerut E, van Erp F, Hoogerbrugge N, van Kempen L, Schoenmakers EF, Bonne A, Maher ER, Geurts van Kessel A. Kuiper RP, et al. Among authors: govaerts l. Cancer Genet Cytogenet. 2009 Dec;195(2):105-11. doi: 10.1016/j.cancergencyto.2009.07.001. Cancer Genet Cytogenet. 2009. PMID: 19963109

5

[Before and after chorionic villi sampling].

Mantingh A, Breed AS, Boogert A, Govaerts LC. Mantingh A, et al. Among authors: govaerts lc. Ned Tijdschr Geneeskd. 1986 Jul 19;130(29):1327-9. Ned Tijdschr Geneeskd. 1986. PMID: 3748214 Dutch. No abstract available.

6

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

7

Inversion duplication of the short arm of chromosome 8: clinical data on seven patients and review of the literature.

de Die-Smulders CE, Engelen JJ, Schrander-Stumpel CT, Govaerts LC, de Vries B, Vles JS, Wagemans A, Schijns-Fleuren S, Gillessen-Kaesbach G, Fryns JP. de Die-Smulders CE, et al. Among authors: govaerts lc. Am J Med Genet. 1995 Nov 20;59(3):369-74. doi: 10.1002/ajmg.1320590318. Am J Med Genet. 1995. PMID: 8599364 Review.

8

Submicroscopic Xpter deletion in a boy with growth and mental retardation caused by a familial t(X;14).

de Vries BB, Eussen BH, van Diggelen OP, van Der Heide A, Deelen WH, Govaerts LC, Lindhout D, Wouters CH, Van Hemel JO. de Vries BB, et al. Among authors: govaerts lc. Am J Med Genet. 1999 Nov 19;87(2):189-94. doi: 10.1002/(sici)1096-8628(19991119)87:2<189::aid-ajmg12>3.3.co;2-h. Am J Med Genet. 1999. PMID: 10533035

9

Mosaic tetrasomy 8p in two patients: clinical data and review of the literature.

Schrander-Stumpel CT, Govaerts LC, Engelen JJ, van der Blij-Philipsen M, Borghgraef M, Loots WJ, Peters JJ, Rijnvos WP, Smeets DF, Fryns JP. Schrander-Stumpel CT, et al. Among authors: govaerts lc. Am J Med Genet. 1994 May 1;50(4):377-80. doi: 10.1002/ajmg.1320500416. Am J Med Genet. 1994. PMID: 7516121 Review.

10

Familial insertion (3;5)(q25.3;q22.1q31.3) with deletion or duplication of chromosome region 5q22.1-5q31.3 in ten unbalanced carriers.

Arens YH, Engelen JJ, Govaerts LC, van Ravenswaay CM, Loneus WH, van Lent-Albrechts JC, van der Blij-Philipsen M, Hamers AJ, Schrander-Stumpel CT. Arens YH, et al. Among authors: govaerts lc. Am J Med Genet A. 2004 Oct 1;130A(2):128-33. doi: 10.1002/ajmg.a.20568. Am J Med Genet A. 2004. PMID: 15372532

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