Hoovers JM - Search Results

1

Isolation and characterization of the human SCP2 cDNA and chromosomal localization of the gene.

Schalk JA, Offenberg HH, Peters E, Groot NP, Hoovers JM, Heyting C. Schalk JA, et al. Among authors: hoovers jm. Mamm Genome. 1999 Jun;10(6):642-4. doi: 10.1007/s003359901062. Mamm Genome. 1999. PMID: 10341103 No abstract available.

2

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: hoovers jm. Genomics. 1997 Feb 1;39(3):377-84. doi: 10.1006/geno.1996.4373. Genomics. 1997. PMID: 9119375

3

Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family.

Mannens M, Bleeker-Wagemakers EM, Bliek J, Hoovers J, Mandjes I, van Tol S, Frants RR, Heyting C, Westerveld A, Slater RM. Mannens M, et al. Cytogenet Cell Genet. 1989;52(1-2):32-6. doi: 10.1159/000132834. Cytogenet Cell Genet. 1989. PMID: 2575483

4

An integrated map of chromosome 18 CAG trinucleotide repeat loci.

Grierson AJ, van Groenigen M, Groot NP, Lindblad K, Hoovers JM, Schalling M, de Belleroche J, Baas F. Grierson AJ, et al. Among authors: hoovers jm. Eur J Hum Genet. 1999 Jan;7(1):12-9. doi: 10.1038/sj.ejhg.5200246. Eur J Hum Genet. 1999. PMID: 10094186

5

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. J Gen Virol. 1988 Feb;69 ( Pt 2):467-71. doi: 10.1099/0022-1317-69-2-467. J Gen Virol. 1988. PMID: 2828520

6

FISH mapping of three ammonia metabolism genes (Glul, Cps1, Glud1) in rat, and the chromosomal localization of GLUL in human and Cps1 in mouse.

Helou K, Das AT, Lamers WH, Hoovers JM, Szpirer C, Szpirer J, Klinga-Levan K, Levan G. Helou K, et al. Among authors: hoovers jm. Mamm Genome. 1997 May;8(5):362-4. doi: 10.1007/s003359900442. Mamm Genome. 1997. PMID: 9107685 No abstract available.

7

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. Genomics. 1993 Mar;15(3):525-9. doi: 10.1006/geno.1993.1104. Genomics. 1993. PMID: 8468047

8

Common missense mutation G1528C in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Characterization and expression of the mutant protein, mutation analysis on genomic DNA and chromosomal localization of the mitochondrial trifunctional protein alpha subunit gene.

IJlst L, Ruiter JP, Hoovers JM, Jakobs ME, Wanders RJ. IJlst L, et al. Among authors: hoovers jm. J Clin Invest. 1996 Aug 15;98(4):1028-33. doi: 10.1172/JCI118863. J Clin Invest. 1996. PMID: 8770876 Free PMC article.

9

Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3.

Redeker E, Alders M, Hoovers JM, Richard CW 3rd, Westerveld A, Mannens M. Redeker E, et al. Among authors: hoovers jm. Cytogenet Cell Genet. 1995;68(3-4):222-5. doi: 10.1159/000133917. Cytogenet Cell Genet. 1995. PMID: 7842740

10

A patient with a de novo t (6;9) and an interstitial duplication of (9)(q21.2q22.1).

Mohrschladt MF, Bijlsma EK, Sluijter S, De Coo RF, Hoovers JM, Leschot NJ. Mohrschladt MF, et al. Among authors: hoovers jm. Clin Dysmorphol. 1999 Jul;8(3):211-4. Clin Dysmorphol. 1999. PMID: 10457857

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