| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A submicroscopic unbalanced subtelomeric translocation t(2p;10q) identified by fluorescence in situ hybridization: fetus with increased nuchal translucency and normal standard karyotype with later growth and developmental delay, rhombencephalosynapsis (RES)
|
Lespinasse, J.
|
|
2004
|
47 |
4 |
p. 405-417
13 p.
|
artikel
|
| 2 |
Author index
|
|
|
2004
|
47 |
4 |
p. 439-441
3 p.
|
artikel
|
| 3 |
Contribution of ultrasonographic examination to the prenatal detection of trisomy 21: experience from 19 European registers
|
Wellesley, D.
|
|
2004
|
47 |
4 |
p. 373-380
8 p.
|
artikel
|
| 4 |
Cryptic translocations involving chromosome 20 in polycythemia vera
|
Busson, Maryvonne
|
|
2004
|
47 |
4 |
p. 365-371
7 p.
|
artikel
|
| 5 |
CV2 Editorial Board redaction
|
|
|
2004
|
47 |
4 |
p. IFC-
1 p.
|
artikel
|
| 6 |
DNA polymorphism analysis of candidate genes for type 2 diabetes mellitus in a Mexican ethnic group
|
Flores-Martínez, S.E.
|
|
2004
|
47 |
4 |
p. 339-348
10 p.
|
artikel
|
| 7 |
Effect of 5637 conditioned medium (CM) on the mitotic index in the cytogenetic evaluation of myeloproliferative disorders
|
Gozzetti, Alessandro
|
|
2004
|
47 |
4 |
p. 432-434
3 p.
|
artikel
|
| 8 |
Genotypic analysis of the TGF beta-509 allele in patients with systemic lupus erythematosus and Sjögren's syndrome
|
Caserta, Tina M.
|
|
2004
|
47 |
4 |
p. 359-363
5 p.
|
artikel
|
| 9 |
In memoriam : Jean de Grouchy, 1926–2003
|
Turleau, Catherine
|
|
2004
|
47 |
4 |
p. 435-437
3 p.
|
artikel
|
| 10 |
Intranuclear arrangement of human chromosome 12 is reflected in metaphase chromosomes as non-random bending
|
Plaja, A.
|
|
2004
|
47 |
4 |
p. 429-432
4 p.
|
artikel
|
| 11 |
Isolated congenital anonychia cases with coincident chromosomal fragility
|
Özyazgan, İrfan
|
|
2004
|
47 |
4 |
p. 381-386
6 p.
|
artikel
|
| 12 |
Keyword index
|
|
|
2004
|
47 |
4 |
p. 443-450
8 p.
|
artikel
|
| 13 |
Large duplication 4q25–q34 with mild clinical effect
|
Elghezal, Hatem
|
|
2004
|
47 |
4 |
p. 419-422
4 p.
|
artikel
|
| 14 |
Non-lethal Hallermann–Streiff syndrome with bone fracture: report of a case
|
Ertekin, Vildan
|
|
2004
|
47 |
4 |
p. 387-391
5 p.
|
artikel
|
| 15 |
Partial trisomy 8q and partial monosomy 18p: a case report
|
Puvabanditsin, S.
|
|
2004
|
47 |
4 |
p. 399-403
5 p.
|
artikel
|
| 16 |
Partial trisomy 18q11.2→qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization
|
Semerci, C.Nur
|
|
2004
|
47 |
4 |
p. 393-398
6 p.
|
artikel
|
| 17 |
Prevalence of C282Y and H63D mutations in the haemochromatosis (HFE) gene in Tunisian population
|
Sassi, R.
|
|
2004
|
47 |
4 |
p. 325-330
6 p.
|
artikel
|
| 18 |
The peptide nucleic acids (PNAs): a new generation of probes for genetic and cytogenetic analyses
|
Paulasova, Petra
|
|
2004
|
47 |
4 |
p. 349-358
10 p.
|
artikel
|
| 19 |
Trisomy 4 associated with double minute chromosomes and MYC amplification in acute myeloblastic leukemia
|
Receveur, Aline
|
|
2004
|
47 |
4 |
p. 423-427
5 p.
|
artikel
|
| 20 |
Y chromosome micro-deletions in idiopathic infertility from Northern India
|
Mittal, Rama Devi
|
|
2004
|
47 |
4 |
p. 331-337
7 p.
|
artikel
|
Tijdschrift beschrijving