| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Announcing a new Editor-in-Chief and a new name
|
|
|
2005
|
48 |
1 |
p. 3-
1 p.
|
artikel
|
| 2 |
Atypical 18p- syndrome associated with partial trisomy 16p in a chromosomally unbalanced child of consanguineous parents with an identical balanced translocation
|
Kupchik, Gabriel S.
|
|
2005
|
48 |
1 |
p. 57-65
9 p.
|
artikel
|
| 3 |
CV2 Editorial Board redaction
|
|
|
2005
|
48 |
1 |
p. CO2-
1 p.
|
artikel
|
| 4 |
Double aneuploidy involving trisomy 7 with Potter sequence
|
Biri, Aydan
|
|
2005
|
48 |
1 |
p. 67-73
7 p.
|
artikel
|
| 5 |
Double aneuploidy mosaicism with Down–Klinefelter’s syndrome
|
Bianca, S.
|
|
2005
|
48 |
1 |
p. 75-76
2 p.
|
artikel
|
| 6 |
FISH approach to determine cat eye syndrome chromosome breakpoints of a patient with cat eye syndrome type II
|
Gentile, M.
|
|
2005
|
48 |
1 |
p. 33-39
7 p.
|
artikel
|
| 7 |
Haplotypes Eco47 III–Nsp I sites frequencies on the IDUA gene in Mexican native population
|
Gallegos-Arreola, M.P.
|
|
2005
|
48 |
1 |
p. 29-32
4 p.
|
artikel
|
| 8 |
Interphase-FISH study in three patients with tetraploid/diploid mosaicism
|
Cavalcanti, Denise P.
|
|
2005
|
48 |
1 |
p. 41-50
10 p.
|
artikel
|
| 9 |
[No title]
|
Stoll, Claude
|
|
2005
|
48 |
1 |
p. 77-
1 p.
|
artikel
|
| 10 |
[No title]
|
Stoll, Claude
|
|
2005
|
48 |
1 |
p. 78-
1 p.
|
artikel
|
| 11 |
[No title]
|
Devriendt, Koen
|
|
2005
|
48 |
1 |
p. 1-
1 p.
|
artikel
|
| 12 |
Polycystic kidneys and del (4)(q21.1q21.3): further delineation of a distinct phenotype
|
Velinov, M.
|
|
2005
|
48 |
1 |
p. 51-55
5 p.
|
artikel
|
| 13 |
The prevalence of major congenital malformations during two periods of time, 1986–1994 and 1995–2002 in newborns conceived by assisted reproduction technology
|
Merlob, Paul
|
|
2005
|
48 |
1 |
p. 5-11
7 p.
|
artikel
|
| 14 |
The role of genetic counseling on decisions of pregnant women aged 35 years or over regarding amniocentesis in Turkey
|
Ilgın-Ruhi, Hatice
|
|
2005
|
48 |
1 |
p. 13-19
7 p.
|
artikel
|
| 15 |
Vitamin E deficiency ataxia with (744 del A) mutation on α-TTP gene: genetic and clinical peculiarities in Moroccan patients
|
Marzouki, Naima
|
|
2005
|
48 |
1 |
p. 21-28
8 p.
|
artikel
|
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