Leschot NJ - Search Results

1

High-resolution localization of 69 potential human zinc finger protein genes: a number are clustered.

Hoovers JM, Mannens M, John R, Bliek J, van Heyningen V, Porteous DJ, Leschot NJ, Westerveld A, Little PF. Hoovers JM, et al. Among authors: leschot nj. Genomics. 1992 Feb;12(2):254-63. doi: 10.1016/0888-7543(92)90372-y. Genomics. 1992. PMID: 1740334

2

High-resolution chromosomal localization of the human calcitonin/CGRP/IAPP gene family members.

Hoovers JM, Redeker E, Speleman F, Höppener JW, Bhola S, Bliek J, van Roy N, Leschot NJ, Westerveld A, Mannens M. Hoovers JM, et al. Among authors: leschot nj. Genomics. 1993 Mar;15(3):525-9. doi: 10.1006/geno.1993.1104. Genomics. 1993. PMID: 8468047

3

Human synaptonemal complex protein 1 (SCP1): isolation and characterization of the cDNA and chromosomal localization of the gene.

Meuwissen RL, Meerts I, Hoovers JM, Leschot NJ, Heyting C. Meuwissen RL, et al. Among authors: leschot nj. Genomics. 1997 Feb 1;39(3):377-84. doi: 10.1006/geno.1996.4373. Genomics. 1997. PMID: 9119375

4

Reduced copy number of DAZ genes in subfertile and infertile men.

de Vries JW, Hoffer MJ, Repping S, Hoovers JM, Leschot NJ, van der Veen F. de Vries JW, et al. Among authors: leschot nj. Fertil Steril. 2002 Jan;77(1):68-75. doi: 10.1016/s0015-0282(01)02935-1. Fertil Steril. 2002. PMID: 11779593 Free article.

5

Supernumerary ring chromosome 20 characterized by fluorescence in situ hybridization.

van Langen IM, Otter MA, Aronson DC, Overweg-Plandsoen WC, Hennekam RC, Leschot NJ, Hoovers JM. van Langen IM, et al. Among authors: leschot nj. Clin Genet. 1996 Jan;49(1):49-53. doi: 10.1111/j.1399-0004.1996.tb04325.x. Clin Genet. 1996. PMID: 8721573

6

Further delineation of the partial proximal trisomy 10q syndrome.

Aalfs CM, Hoovers JM, Nieste-Otter MA, Mannens MM, Hennekam RC, Leschot NJ. Aalfs CM, et al. Among authors: leschot nj. J Med Genet. 1995 Dec;32(12):968-71. doi: 10.1136/jmg.32.12.968. J Med Genet. 1995. PMID: 8825926 Free PMC article.

7

[Fluorescence in situ hybridization in the study of chromosomal abnormalities].

Hoovers JM, Mellink CH, Leschot NJ. Hoovers JM, et al. Among authors: leschot nj. Ned Tijdschr Geneeskd. 1999 Nov 6;143(45):2265-8. Ned Tijdschr Geneeskd. 1999. PMID: 10578427 Review. Dutch.

8

Morphological transformation by early region human polyomavirus BK DNA of human fibroblasts with deletions in the short arm of one chromosome 11.

de Ronde A, Mannens M, Slater RM, Hoovers J, Heyting C, Bleeker-Wagemakers EM, Leschot NJ, van Strien A, Sol CJ, ter Schegget J, et al. de Ronde A, et al. Among authors: leschot nj. J Gen Virol. 1988 Feb;69 ( Pt 2):467-71. doi: 10.1099/0022-1317-69-2-467. J Gen Virol. 1988. PMID: 2828520

9

[Decoding of the human genome: a milestone, but not the end of the road].

Leschot NJ, Mannens MM. Leschot NJ, et al. Ned Tijdschr Geneeskd. 2000 Jun 3;144(23):1093-6. Ned Tijdschr Geneeskd. 2000. PMID: 10876702 Review. Dutch.

10

Enrichment, identification and analysis of fetal cells from maternal blood: evaluation of a prenatal diagnosis system.

de Graaf IM, Jakobs ME, Leschot NJ, Ravkin I, Goldbard S, Hoovers JM. de Graaf IM, et al. Among authors: leschot nj. Prenat Diagn. 1999 Jul;19(7):648-52. doi: 10.1002/(sici)1097-0223(199907)19:7<648::aid-pd600>3.0.co;2-x. Prenat Diagn. 1999. PMID: 10419613

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