16 results on '"Vekemans M"'
Search Results
2. OFD1 mutations in males: phenotypic spectrum and ciliary basal body docking impairment
3. Monozygotic twins discordant for submicroscopic chromosomal anomalies in 2p25.3 region detected by array CGH
4. Sotos syndrome caused by a paracentric inversion disrupting the NSD1 gene
5. Chimera and other fertilization errors
6. Genome-wide screening using automated fluorescent genotyping to detect cryptic cytogenetic abnormalities in children with idiopathic syndromic mental retardation
7. PMX2B, a new candidate gene for Hirschsprungʼs disease
8. A CGH study of 27 patients with CHARGE association
9. Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotype
10. Wilms' tumor and gonadal dysgenesis in a child with the 2q37.1 deletion syndrome
11. Xq25 duplication: the crucial role of the STAG2 gene in this novel human cohesinopathy
12. Monozygotic twins discordant for submicroscopic chromosomal anomalies in 2p25.3 region detected by array CGH
13. OFD1mutations in males: phenotypic spectrum and ciliary basal body docking impairment
14. Wilms' tumor and gonadal dysgenesis in a child with the 2q37.1 deletion syndrome
15. Sotos syndrome caused by a paracentric inversion disrupting the NSD1 gene
16. Down syndrome patients are less likely to develop some (but not all) malignant solid tumours.
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