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K Devriendt

Showing results (91-100 of 230) with videos related to

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Genetic Counseling (Geneva, Switzerland)|April 7, 1999
Retrospective analysis of feeding and speech disorders in 50 patients with velo-cardio-facial syndromeN Rommel, G Vantrappen, A Swillen, et al.
European Journal of Pediatrics|August 1, 1996
The incidence of a deletion in chromosome 22Q11 in sporadic and familial conotruncal heart diseaseK Devriendt, B Eyskens, A Swillen, et al.
Molecular Syndromology|April 19, 2012
Differences in Copy Number Variation between Discordant Monozygotic Twins as a Model for Exploring Chromosomal Mosaicism in Congenital Heart DefectsJ Breckpot, B Thienpont, M Gewillig, et al.
Cancer Genetics and Cytogenetics|April 1, 1990
Chromosome mapping using polymerase chain reaction on somatic cell hybridsJ Zhang, K Devriendt, P Marynen, et al.
Journal of Medical Genetics|September 11, 1998
The annual incidence of DiGeorge/velocardiofacial syndromeK Devriendt, J P Fryns, G Mortier, et al.
Orthodontics & Craniofacial Research|January 18, 2008
Investigating the etiology of multiple tooth agenesis in three sisters with severe oligodontiaS Swinnen, I Bailleul-Forestier, S Arte, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Wiedemann-Beckwith syndrome and chromosomal duplication 4q/deficiency 18pJ P Fryns, A Kleczkowska, K Devriendt, et al.
JBR-BTR : Organe De La Societe Royale Belge De Radiologie (SRBR) = Orgaan Van De Koninklijke Belgische Vereniging Voor Radiologie (KBVR)|July 31, 2014
Unilateral giant cell lesion of the jaw in Noonan syndromeM Eyselbergs, F Vanhoenacker, J Hintjens, et al.
Ophthalmic Genetics|April 21, 2016
Posterior amorphous corneal dystrophy caused by a de novo deletionS Odent, I Casteels, C Cassiman, et al.
Biochemical and Biophysical Research Communications|April 30, 1992
Structure of the human alpha-2 macroglobulin gene and its promotorG Matthijs, K Devriendt, J J Cassiman, et al.
Pageof 23

Showing results (91-100 of 230) with videos related to

Sort By:
Pageof 23
Genetic Counseling (Geneva, Switzerland)|April 7, 1999
Retrospective analysis of feeding and speech disorders in 50 patients with velo-cardio-facial syndromeN Rommel, G Vantrappen, A Swillen, et al.
European Journal of Pediatrics|August 1, 1996
The incidence of a deletion in chromosome 22Q11 in sporadic and familial conotruncal heart diseaseK Devriendt, B Eyskens, A Swillen, et al.
Molecular Syndromology|April 19, 2012
Differences in Copy Number Variation between Discordant Monozygotic Twins as a Model for Exploring Chromosomal Mosaicism in Congenital Heart DefectsJ Breckpot, B Thienpont, M Gewillig, et al.
Cancer Genetics and Cytogenetics|April 1, 1990
Chromosome mapping using polymerase chain reaction on somatic cell hybridsJ Zhang, K Devriendt, P Marynen, et al.
Journal of Medical Genetics|September 11, 1998
The annual incidence of DiGeorge/velocardiofacial syndromeK Devriendt, J P Fryns, G Mortier, et al.
Orthodontics & Craniofacial Research|January 18, 2008
Investigating the etiology of multiple tooth agenesis in three sisters with severe oligodontiaS Swinnen, I Bailleul-Forestier, S Arte, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1993
Wiedemann-Beckwith syndrome and chromosomal duplication 4q/deficiency 18pJ P Fryns, A Kleczkowska, K Devriendt, et al.
JBR-BTR : Organe De La Societe Royale Belge De Radiologie (SRBR) = Orgaan Van De Koninklijke Belgische Vereniging Voor Radiologie (KBVR)|July 31, 2014
Unilateral giant cell lesion of the jaw in Noonan syndromeM Eyselbergs, F Vanhoenacker, J Hintjens, et al.
Ophthalmic Genetics|April 21, 2016
Posterior amorphous corneal dystrophy caused by a de novo deletionS Odent, I Casteels, C Cassiman, et al.
Biochemical and Biophysical Research Communications|April 30, 1992
Structure of the human alpha-2 macroglobulin gene and its promotorG Matthijs, K Devriendt, J J Cassiman, et al.
Pageof 23