| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A constitutional translocation t(1;4)(p21;p15) in a case of chronic lymphocytic leukemia
|
Eclache, Virginie
|
|
2002
|
45 |
4 |
p. 169-171
3 p.
|
artikel
|
| 2 |
A family with two different chromosomal translocations
|
Ozkul, Y.
|
|
2002
|
45 |
4 |
p. 185-187
3 p.
|
artikel
|
| 3 |
A Turner patient with a 45,X,t(1;2) (q41;p11.2) karyotype
|
Ozkul, Yusuf
|
|
2002
|
45 |
4 |
p. 181-183
3 p.
|
artikel
|
| 4 |
Auricular mild errors of morphogenesis: epidemiological study with application of a targeted computer program
|
Grun, Marta
|
|
2002
|
45 |
4 |
p. 207-212
6 p.
|
artikel
|
| 5 |
Chromosome studies of in vitro senescent lymphocytes: nonrandom trisomy 2
|
Busson-Le Coniat, Maryvonne
|
|
2002
|
45 |
4 |
p. 193-196
4 p.
|
artikel
|
| 6 |
Distal trisomy 14 (q24 → qter) and aorto-pulmonary window: a case report and review of the literature
|
Perrin, Yannick
|
|
2002
|
45 |
4 |
p. 173-175
3 p.
|
artikel
|
| 7 |
GM polymorphism and the evolutionary history of modern humans
|
Chaabani, Hassen
|
|
2002
|
45 |
4 |
p. 197-206
10 p.
|
artikel
|
| 8 |
Haploinsufficiency of TBX3 causes ulnar-mammary syndrome in a large Turkish family
|
Wollnik, Bernd
|
|
2002
|
45 |
4 |
p. 213-217
5 p.
|
artikel
|
| 9 |
Screening for mutations in the gene for phosphorylation kinase γ1 in Silver–Russell syndrome patients
|
Mavany, Miriam
|
|
2002
|
45 |
4 |
p. 219-221
3 p.
|
artikel
|
| 10 |
Tetraploid/diploid mosaicism: case report and review of the literature
|
Alonso, Luís
|
|
2002
|
45 |
4 |
p. 177-180
4 p.
|
artikel
|
| 11 |
Use of two FISH probes provides a cost-effective, simple protocol to exclude an imprinting centre defect in routine laboratory testing for suspected Prader–Willi and Angelman syndrome
|
Smith, Arabella
|
|
2002
|
45 |
4 |
p. 189-191
3 p.
|
artikel
|
Tijdschrift beschrijving