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                             19 gevonden resultaten
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
                             19 gevonden resultaten
 
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