| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A case of (X;15) translocation diagnosed as a paracentric inversion of Xp: diagnostic revision with FISH
|
Paoloni-Giacobino, A
|
|
2001
|
44 |
3 |
p. 117-119
3 p.
|
artikel
|
| 2 |
A complex chromosome rearrangement involving chromosome 8, 11, and 12 analyzed by conventional cytogenetic investigations, fluorescence in situ hybridisation, and spectral karyotyping
|
Kotzot, D
|
|
2001
|
44 |
3 |
p. 135-138
4 p.
|
artikel
|
| 3 |
Carrier detection and prenatal molecular diagnosis in a Duchenne muscular dystrophy family without any affected relative available
|
Alcántara, M.A
|
|
2001
|
44 |
3 |
p. 149-153
5 p.
|
artikel
|
| 4 |
Cytogenetics of Neuroblastoma : A Study Using Fine Needle Aspiration Cultures
|
Udayakumar, A.M.
|
|
2001
|
44 |
3 |
p. 161-166
6 p.
|
artikel
|
| 5 |
Deletion of 2q37 and duplication of 10q24: Two cases in the same family and review of the literature
|
Wiktor, A.
|
|
2001
|
44 |
3 |
p. 129-134
6 p.
|
artikel
|
| 6 |
Heteromorphism 18ph+ : with or without reproductive consequences ?
|
Tabet, A.C.
|
|
2001
|
44 |
3 |
p. 139-142
4 p.
|
artikel
|
| 7 |
Molecular analysis of SRY gene in patients with mixed gonadal dysgenesis
|
Álvarez-Nava, Francisco
|
|
2001
|
44 |
3 |
p. 155-159
5 p.
|
artikel
|
| 8 |
Mosaic trisomy 15 and hemihypertrophy
|
Gérard-Blanluet, Marion
|
|
2001
|
44 |
3 |
p. 143-148
6 p.
|
artikel
|
| 9 |
Reduction in the DAZ gene copy number in two infertile men with impaired spermatogenesis
|
Bienvenu, Thierry
|
|
2001
|
44 |
3 |
p. 125-128
4 p.
|
artikel
|
| 10 |
Syndrome of renal, genital and feet malformations
|
Bianca, Sebastiano
|
|
2001
|
44 |
3 |
p. 121-123
3 p.
|
artikel
|
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