J M Hoovers
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Explore the profile of J M Hoovers including associated specialties, affiliations and a list of published articles.
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Citations
489
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Recent Articles
1.
Schuring-Blom G, Hoovers J, van Lith J, Knegt A, Leschot N
Prenat Diagn
. 2001 Dec;
21(10):864-7.
PMID: 11746131
Objective: In chorionic villus sampling (CVS) the chromosome analysis is inconclusive in 1-2% of the samples. In many cases follow-up amniocentesis is performed. Fetal nucleated red blood cells (FNRBCs) are...
2.
Jakobs M, van Lith J, de Graaf I, Knegt A, Hoovers J
Prenat Diagn
. 2000 Oct;
20(10):832-4.
PMID: 11038464
Chorionic villus sampling (CVS) is an established invasive prenatal diagnostic method for the detection of fetal chromosome aberrations. In 1-2% the karyotype result of CVS is inconclusive and follow-up confirmation...
3.
Kleefstra T, van de Zande G, Merkx G, Mieloo H, Hoovers J, Smeets D
Eur J Hum Genet
. 2000 Aug;
8(8):637-40.
PMID: 10951526
Recently, much attention has been given to subtelomeric chromosomal rearrangements as important aetiological factors leading to idiopathic mental retardation. However, detection of these aberrations is difficult, mostly due to technical...
4.
Saxena R, de Vries J, Repping S, Alagappan R, Skaletsky H, Brown L, et al.
Genomics
. 2000 Aug;
67(3):256-67.
PMID: 10936047
The DAZ genes are candidate fertility factors that lie within the human Y chromosome's AZFc region, whose deletion is a common cause of spermatogenic failure. The number of DAZ genes...
5.
Maas S, Hoovers J, van Seggelen M, Menzel D, Hennekam R
Clin Dysmorphol
. 2000 Jan;
9(1):47-53.
PMID: 10649798
We report on a boy with an interstitial deletion of the long arm of chromosome 2 with breakpoints in chromosome bands q23 and q24.3. Main features were low-set and malformed...
6.
Hoovers J, Mellink C, Leschot N
Ned Tijdschr Geneeskd
. 1999 Dec;
143(45):2265-8.
PMID: 10578427
Classical cytogenetics has a low resolving power and allows analysis of dividing cells only. In fluorescence in situ hybridization (FISH), a DNA fragment is stained with a fluorescent marker, after...
7.
Aalfs C, Hoovers J, Wijburg F
Am J Med Genet
. 1999 Sep;
86(4):398-400.
PMID: 10494099
No abstract available.
8.
Bijlsma E, Aalfs C, Sluitjer S, Oude Luttikhuis M, Trembath R, Hoovers J, et al.
J Med Genet
. 1999 Aug;
36(8):604-9.
PMID: 10465110
Recently five patients with an Albright hereditary osteodystrophy (AHO)-like phenotype were reported to have a subtelomeric deletion of the long arm of chromosome 2. These patients showed a striking resemblance...
9.
Mohrschladt M, Bijlsma E, Sluijter S, de Coo R, Hoovers J, Leschot N
Clin Dysmorphol
. 1999 Aug;
8(3):211-4.
PMID: 10457857
We report on a 4-year-old child with psychomotor retardation, general hypotonia and only mild dysmorphic features. Her chromosome constitution was 46,XX, t (6;9) (q27;q22.1), dup (9) (q21.2q22.1). This de novo...
10.
de Graaf I, Jakobs M, Leschot N, Ravkin I, Goldbard S, Hoovers J
Prenat Diagn
. 1999 Jul;
19(7):648-52.
PMID: 10419613
In this study we evaluated the performance of a system for the enrichment, identification and analysis of fetal cells in maternal peripheral blood. Blood samples were collected from women after...