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 |