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K Devriendt

Showing results (21-30 of 230) with videos related to

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Physical Review. E|January 20, 2018
Pseudoinverse of the Laplacian and best spreader node in a networkP Van Mieghem, K Devriendt, H Cetinay
Genetic Counseling (Geneva, Switzerland)|July 17, 1998
Skin pigmentation anomalies in ring chromosome 13J P Fryns, K Devriendt, E Legius
Annales De Genetique|August 6, 1999
A 3p deletion syndrome in a child with both del(3)(p25-->pter) and dup(17)(q23-->qter)T Lukusa, K Devriendt, J P Fryns
Prenatal Diagnosis|July 17, 1998
The prenatal diagnosis of spinal muscular atrophyG Matthijs, K Devriendt, J P Fryns
Genetic Counseling (Geneva, Switzerland)|November 6, 2001
Further evidence for germinal mosaicism in cleft hand/cleft foot syndrome. Two affected halfsisters and normal fatherL De Smet, K Devriendt, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Craniofrontonasal dysplasia: more severe expression in the mother than in her sonK Devriendt, C Van Mol, J P Fryns
Bulletin De La Societe Belge D'Ophtalmologie|November 19, 2003
Heterochromia of the irides and a motility disorder of the oesophagus: a coincidence or a defect during embryogenesis?S Goethals, I Hoffman, K Devriendt, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Hydrocephalus with features of VATERK Devriendt, P De Cock, J P Fryns
Clinical Dysmorphology|June 3, 2005
Scalp skin lesion in Turner syndrome: more than lymphoedema?A Debeer, E Steenkiste, K Devriendt, et al.
Journal of Medical Genetics|July 25, 1998
Holoprosencephaly in deletions of proximal chromosome 14qK Devriendt, J P Fryns, C P Chen
Pageof 23

Showing results (21-30 of 230) with videos related to

Sort By:
Pageof 23
Physical Review. E|January 20, 2018
Pseudoinverse of the Laplacian and best spreader node in a networkP Van Mieghem, K Devriendt, H Cetinay
Genetic Counseling (Geneva, Switzerland)|July 17, 1998
Skin pigmentation anomalies in ring chromosome 13J P Fryns, K Devriendt, E Legius
Annales De Genetique|August 6, 1999
A 3p deletion syndrome in a child with both del(3)(p25-->pter) and dup(17)(q23-->qter)T Lukusa, K Devriendt, J P Fryns
Prenatal Diagnosis|July 17, 1998
The prenatal diagnosis of spinal muscular atrophyG Matthijs, K Devriendt, J P Fryns
Genetic Counseling (Geneva, Switzerland)|November 6, 2001
Further evidence for germinal mosaicism in cleft hand/cleft foot syndrome. Two affected halfsisters and normal fatherL De Smet, K Devriendt, J P Fryns
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Craniofrontonasal dysplasia: more severe expression in the mother than in her sonK Devriendt, C Van Mol, J P Fryns
Bulletin De La Societe Belge D'Ophtalmologie|November 19, 2003
Heterochromia of the irides and a motility disorder of the oesophagus: a coincidence or a defect during embryogenesis?S Goethals, I Hoffman, K Devriendt, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1995
Hydrocephalus with features of VATERK Devriendt, P De Cock, J P Fryns
Clinical Dysmorphology|June 3, 2005
Scalp skin lesion in Turner syndrome: more than lymphoedema?A Debeer, E Steenkiste, K Devriendt, et al.
Journal of Medical Genetics|July 25, 1998
Holoprosencephaly in deletions of proximal chromosome 14qK Devriendt, J P Fryns, C P Chen
Pageof 23