van den Berghe J - Search Results

1

Increased incidence of spontaneous apoptosis in the bone marrow of hyperdiploid childhood acute lymphoblastic leukemia.

Zhang Y, Lu J, van den Berghe J, Lee SH. Zhang Y, et al. Among authors: van den berghe j. Exp Hematol. 2002 Apr;30(4):333-9. doi: 10.1016/s0301-472x(02)00771-3. Exp Hematol. 2002. PMID: 11937268 Free article.

2

Static cytometry identifies hyperdiploid childhood ALL.

van den Berghe JA, Chen YC, Zhang Y, Kueh YK, Lee SH. van den Berghe JA, et al. Cancer Genet Cytogenet. 2000 Dec;123(2):123-7. doi: 10.1016/s0165-4608(00)00312-5. Cancer Genet Cytogenet. 2000. PMID: 11156737

3

Three infants having null acute lymphoblastic leukemia with chromosome rearrangements at 11q23: no involvement of a heritable fragile site in this band.

van den Berghe JA, Malcolm S, Katz FE, Gibbons B, Czepulkowski B, Chessells JM. van den Berghe JA, et al. Cytogenet Cell Genet. 1989;50(1):61-4. doi: 10.1159/000132721. Cytogenet Cell Genet. 1989. PMID: 2743821

4

Regional chromosomal localisation of APOA2 to 1q21-1q23.

Middleton-Price HR, van den Berghe JA, Scott J, Knott TJ, Malcolm S. Middleton-Price HR, et al. Among authors: van den berghe ja. Hum Genet. 1988 Jul;79(3):283-5. doi: 10.1007/BF00366253. Hum Genet. 1988. PMID: 3136074

5

Rapid sexing of human embryos by non-radioactive in situ hybridization: potential for preimplantation diagnosis of X-linked disorders.

Penketh RJ, Delhanty JD, van den Berghe JA, Finklestone EM, Handyside AH, Malcolm S, Winston RM. Penketh RJ, et al. Among authors: van den berghe ja. Prenat Diagn. 1989 Jul;9(7):489-99. doi: 10.1002/pd.1970090706. Prenat Diagn. 1989. PMID: 2771887

6

The association of Angelman's syndrome with deletions within 15q11-13.

Pembrey M, Fennell SJ, van den Berghe J, Fitchett M, Summers D, Butler L, Clarke C, Griffiths M, Thompson E, Super M. Pembrey M, et al. Among authors: van den berghe j. J Med Genet. 1989 Feb;26(2):73-7. doi: 10.1136/jmg.26.2.73. J Med Genet. 1989. PMID: 2918545 Free PMC article.

7

Dysmorphic sibs trisomic for the region 6q22.1-->6q23.3.

Goh DL, Tan AS, Chen JY, Van Den Berghe JA. Goh DL, et al. Among authors: van den berghe ja. J Med Genet. 2000 Nov;37(11):889-92. doi: 10.1136/jmg.37.11.889. J Med Genet. 2000. PMID: 11185077 Free PMC article. No abstract available.

8

High-resolution in situ hybridization technique using biotinylated NMYC oncogene probe reveals periodic structure of HSRs in human neuroblastoma.

Garson JA, van den Berghe JA, Kemshead JT. Garson JA, et al. Among authors: van den berghe ja. Cytogenet Cell Genet. 1987;45(1):10-5. doi: 10.1159/000132417. Cytogenet Cell Genet. 1987. PMID: 2439257

9

Novel non-isotopic in situ hybridization technique detects small (1 Kb) unique sequences in routinely G-banded human chromosomes: fine mapping of N-myc and beta-NGF genes.

Garson JA, van den Berghe JA, Kemshead JT. Garson JA, et al. Among authors: van den berghe ja. Nucleic Acids Res. 1987 Jun 25;15(12):4761-70. doi: 10.1093/nar/15.12.4761. Nucleic Acids Res. 1987. PMID: 3299258 Free PMC article.

10

N-myc: studies on gene amplification/expression and the development of a non-isotopic technique for gene mapping.

Garson JA, van den Berghe J, Sheppard P, Kemshead JT. Garson JA, et al. Among authors: van den berghe j. Prog Clin Biol Res. 1988;271:151-63. Prog Clin Biol Res. 1988. PMID: 3405998 No abstract available.

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