Search Results - Femke Hannes
- Showing 1 - 4 results of 4
-
1
-
2
Fine-grained facial phenotype–genotype analysis in Wolf–Hirschhorn syndrome by Peter Hammond, Femke Hannes, Michael Suttie, Koenraad Devriendt, Joris Vermeesch, Francesca Faravelli, Francesca Forzano, Susan Parekh, Steven Williams, Dominic McMullan, Sarah T. South, John C. Carey, Oliver Quarrell
Published 2011Artigo -
3
Genotype-phenotype correlation in 21 patients with Wolf-Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH) by Nicole Maas, Griet Van Buggenhout, Femke Hannes, Bernard Thienpont, Damien Sanlaville, Klaas Kok, Alina T. Midro, Joris Andrieux, B-M Anderlid, Jacqueline Schoumans, Roel Hordijk, Koenraad Devriendt, JP Fryns, Joris Vermeesch
Published 2007Artigo -
4
Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant by Femke Hannes, Andrew J. Sharp, Heather C. Mefford, Thomy de Ravel, Claudia Ruivenkamp, M.H. Breuning, JP Fryns, Koenraad Devriendt, Griet Van Buggenhout, Annick Vogels, Helen Stewart, Raoul C. M. Hennekam, Gregory M. Cooper, Regina Regan, Samantha J.L. Knight, Evan E. Eichler, Joris Vermeesch
Published 2008Artigo
Search Tools:
Related Subjects
Biology
Chromosome
Gene
Genetics
Breakpoint
Comparative genomic hybridization
Genotype-phenotype distinction
Microcephaly
Phenotype
Anatomy
Biochemistry
Cell
Cell biology
Cell membrane
Chromosomal inversion
Chromosomal translocation
Chromosome 4
Copy-number variation
Craniofacial
Cytoplasm
Environmental health
Forehead
Gene duplication
Gene family
Genetic recombination
Genome
Glabella
Hypertelorism
Hypospadias
Karyotype