van der Veen AY - Search Results

1

Tetrasomy 5p mosaicism in a boy with delayed growth, hypotonia, minor anomalies, and an additional isochromosome 5p [46,XY/47,XY, + i(5p)].

Sijmons RH, Leegte B, van Lingen RA, de Pater JM, van der Veen AY, del Canho H, Bos C, ten Kate LP, Breed AS. Sijmons RH, et al. Among authors: van der veen ay, van lingen ra. Am J Med Genet. 1993 Sep 15;47(4):559-62. doi: 10.1002/ajmg.1320470424. Am J Med Genet. 1993. PMID: 7504882

2

Tetrasomy 9p due to an intrachromosomal triplication of 9p13-p22.

Verheij JB, Bouman K, van Lingen RA, van Lookeren Campagne JG, Leegte B, van der Veen AY, Hofstra RM, Buys CH, van Essen AJ. Verheij JB, et al. Among authors: van der veen ay. Am J Med Genet. 1999 Sep 10;86(2):168-73. doi: 10.1002/(sici)1096-8628(19990910)86:2<168::aid-ajmg16>3.0.co;2-q. Am J Med Genet. 1999. PMID: 10449655 Review.

3

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

4

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. Among authors: van der veen ay, van aken b. Prenat Diagn. 1995 May;15(5):467-73. doi: 10.1002/pd.1970150510. Prenat Diagn. 1995. PMID: 7644437

5

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. Among authors: van der veen ay. 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

6

Localization of DNA probes with tight linkage to the cystic fibrosis locus by in situ hybridization using fibroblasts with a 7q22 deletion.

van der Hout AH, van der Veen AY, Aten JA, Buys CH. van der Hout AH, et al. Among authors: van der veen ay. Hum Genet. 1988 Oct;80(2):161-4. doi: 10.1007/BF00702861. Hum Genet. 1988. PMID: 3169740

7

Infantile and adult testicular germ cell tumors. a different pathogenesis?

van Echten J, Timmer A, van der Veen AY, Molenaar WM, de Jong B. van Echten J, et al. Among authors: van der veen ay. Cancer Genet Cytogenet. 2002 May;135(1):57-62. doi: 10.1016/s0165-4608(01)00643-4. Cancer Genet Cytogenet. 2002. PMID: 12072204 Review.

8

Localization at a subband level of polymorphic 13q14 DNA probes for diagnosis of hereditary retinoblastoma and Wilson disease.

Scheffer H, Kema IP, Kondo I, van der Veen AY, Ikeuchi T, Buys CH. Scheffer H, et al. Among authors: van der veen ay. Hum Genet. 1987 Dec;77(4):335-7. doi: 10.1007/BF00291421. Hum Genet. 1987. PMID: 2891602

9

Ordering of polymorphic markers in the chromosome region 3p21.

van den Berg A, Kooy RF, Hulsbeek MM, de Jong D, Kok K, van der Veen AY, Buys CH. van den Berg A, et al. Among authors: van der veen ay. Cytogenet Cell Genet. 1996;72(2-3):225-8. doi: 10.1159/000134196. Cytogenet Cell Genet. 1996. PMID: 8978783

10

Physical localisation of the chromosomal marker D13S31 places the Wilson disease locus at the junction of bands q14.3 and q21.1 of chromosome 13.

Kooy RF, Van der Veen AY, Verlind E, Houwen RH, Scheffer H, Buys CH. Kooy RF, et al. Among authors: van der veen ay. Hum Genet. 1993 Jun;91(5):504-6. doi: 10.1007/BF00217780. Hum Genet. 1993. PMID: 8314565

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