| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Announcing “chromosomal imbalance letter”
|
Devriendt, Koenraad
|
|
2005
|
48 |
3 |
p. 353-354
2 p.
|
artikel
|
| 2 |
Application of a comprehensive subtelomere array in clinical diagnosis of mental retardation
|
Kok, Klaas
|
|
2005
|
48 |
3 |
p. 250-262
13 p.
|
artikel
|
| 3 |
CV2 Editorial Board redaction
|
|
|
2005
|
48 |
3 |
p. CO2-
1 p.
|
artikel
|
| 4 |
Detection and delineation of an unusual 17p11.2 deletion by array-CGH and refinement of the Smith–Magenis syndrome minimum deletion to ~650 kb
|
Schoumans, Jacqueline
|
|
2005
|
48 |
3 |
p. 290-300
11 p.
|
artikel
|
| 5 |
From chromosomes to molecular karyotyping
|
Vermeesch, Joris Robert
|
|
2005
|
48 |
3 |
p. 211-213
3 p.
|
artikel
|
| 6 |
High resolution microarray CGH and MLPA analysis for improved genotype/phenotype evaluation of two childhood genetic disorder cases: ring chromosome 19 and partial duplication 2q
|
Hermsen, Mario A.J.A.
|
|
2005
|
48 |
3 |
p. 310-318
9 p.
|
artikel
|
| 7 |
Identification of an unbalanced X-autosome translocation by array CGH in a boy with a syndromic form of chondrodysplasia punctata brachytelephalangic type
|
Menten, Björn
|
|
2005
|
48 |
3 |
p. 301-309
9 p.
|
artikel
|
| 8 |
Interstitial 6q deletion: clinical and array CGH characterisation of a new patient
|
Le Caignec, Cédric
|
|
2005
|
48 |
3 |
p. 339-345
7 p.
|
artikel
|
| 9 |
MAPH: from gels to microarrays
|
Patsalis, Philippos C.
|
|
2005
|
48 |
3 |
p. 241-249
9 p.
|
artikel
|
| 10 |
9 Mb deletion including chromosome band 3q24 associated with unsuspicious facial gestalt, persistent ductus omphaloentericus, mild mental retardation and tic
|
Zweier, Christiane
|
|
2005
|
48 |
3 |
p. 360-362
3 p.
|
artikel
|
| 11 |
25 Mb deletion of 13q13.3→q21.31 in a patient without retinoblastoma
|
Thienpont, Bernard
|
|
2005
|
48 |
3 |
p. 363-366
4 p.
|
artikel
|
| 12 |
Molecular karyotyping in human constitutional cytogenetics
|
Sanlaville, Damien
|
|
2005
|
48 |
3 |
p. 214-231
18 p.
|
artikel
|
| 13 |
Narrowing the deleted region associated with the 15q21 syndrome
|
Pramparo, Tiziano
|
|
2005
|
48 |
3 |
p. 346-352
7 p.
|
artikel
|
| 14 |
Prenatal Diagnosis by Array-CGH
|
Rickman, L.
|
|
2005
|
48 |
3 |
p. 232-240
9 p.
|
artikel
|
| 15 |
Small Reciprocal Insertion detected by Spectral Karyotyping (SKY) and delimited by Array-CGH Analysis
|
Matthaei, Anja
|
|
2005
|
48 |
3 |
p. 328-338
11 p.
|
artikel
|
| 16 |
Tetrasomy 12pter-12p13.31 in a girl with partial Pallister–Killian syndrome phenotype
|
Vermeesch, Joris Robert
|
|
2005
|
48 |
3 |
p. 319-327
9 p.
|
artikel
|
| 17 |
The del(2)(q32.2q33) deletion syndrome defined by clinical and molecular characterization of four patients
|
Van Buggenhout, G.
|
|
2005
|
48 |
3 |
p. 276-289
14 p.
|
artikel
|
| 18 |
Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13
|
de Ravel, Thomy
|
|
2005
|
48 |
3 |
p. 355-359
5 p.
|
artikel
|
| 19 |
X chromosome array-CGH for the identification of novel X-linked mental retardation genes
|
Bauters, Marijke
|
|
2005
|
48 |
3 |
p. 263-275
13 p.
|
artikel
|
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