J C Dreesen
Overview
Explore the profile of J C Dreesen including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
21
Citations
156
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Dreesen J, Jacobs L, Bras M, Herbergs J, Dumoulin J, Geraedts J, et al.
Mol Hum Reprod
. 2000 Apr;
6(5):391-6.
PMID: 10775641
Cystic fibrosis (CF) is the first monogenic disorder for which single cell preimplantation genetic diagnosis (PGD) has been successfully applied. The spectrum of mutations in CF is extremely heterogeneous, and...
2.
de Die-Smulders C, Geraedts J, Dreesen J, Coonen E, Land J
Ned Tijdschr Geneeskd
. 1999 Feb;
142(45):2441-4.
PMID: 10028321
Preimplantation genetic diagnosis (PGD) is a very early form of genetic testing. It involves testing one or two cells taken from a recent embryo of eight cells produced by in...
3.
Dreesen J, Bras M, de Die-Smulders C, Dumoulin J, Cobben J, Evers J, et al.
Mol Hum Reprod
. 1998 Oct;
4(9):881-5.
PMID: 9783849
After Duchenne muscular dystrophy, spinal muscular atrophy (SMA) is the most common severe neuromuscular disease in childhood. Since 1995, homozygous deletions in exon 7 of the survival motor neuron (SMN)...
4.
Coonen E, Dumoulin J, Dreesen J, Bras M, Evers J, Geraedts J
J Assist Reprod Genet
. 1996 Feb;
13(2):133-6.
PMID: 8688585
No abstract available.
5.
Dreesen J, Bras M, Coonen E, Dumoulin J, Evers J, Geraedts J
J Assist Reprod Genet
. 1996 Feb;
13(2):112-4.
PMID: 8688582
No abstract available.
6.
Dreesen J, Geraedts J, Dumoulin J, Evers J, Pieters M
Hum Genet
. 1995 Sep;
96(3):323-9.
PMID: 7649550
In order to approach preimplantation testing for the fragile-X syndrome, we used genotyping of the polymorphic RS46(DXS548) locus closely linked to the FMR-1 gene, in single reproductive cells of females....
7.
Dreesen J, Dumoulin J, Evers J, Geraedts J, Pieters M
Hum Reprod
. 1995 Mar;
10(3):743-8.
PMID: 7782461
Using a multiplex nested polymerase chain reaction (PCR) method with single copy genes and a dinucleotide repeat locus for the mouse Y and X chromosomes respectively, it was possible to...
8.
Dreesen J, SMITS A, van Oost B
Am J Med Genet
. 1994 Jul;
51(4):535-7.
PMID: 7943036
No abstract available.
9.
Dreesen J, van den Hurk J, SMITS A, van den Ouweland A, Markslag P, van Oost B
Hum Genet
. 1993 Mar;
91(1):80-2.
PMID: 8454292
We report a new polymorphic DNA marker (pJH89, DXS539) proximal to the fragile-X site. The pJH89 probe identifies a TaqI and a NcoI restriction fragment length polymorphism (combined heterozygosity of...
10.
SMITS A, Dreesen J, Post J, Smeets D, de Die-Smulders C, Govaerts L, et al.
J Med Genet
. 1993 Feb;
30(2):94-6.
PMID: 8445628
Fragile X (fra(X)) syndrome, the most common form of familial mental retardation, is caused by heritable unstable DNA composed of CGG repeats. As reproductive fitness of fra(X) patients is severely...