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K Devriendt

Showing results (41-50 of 230) with videos related to

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American Journal of Medical Genetics|April 11, 2000
Dicentric chromosome 9 due to tandem duplication of the 9p11-q13 region: unusual chromosome 9 variantT Lukusa, K Devriendt, M Holvoet, et al.
Clinical Genetics|January 1, 1996
Alopecia-mental retardation syndrome associated with convulsions and hypergonadotropic hypogonadismK Devriendt, H Van den Berghe, J P Fryns
Molecular Syndromology|December 6, 2011
FOXD1 Duplication Causes Branchial Defects and Interacts with the TFAP2A Gene Implicated in the Branchio-Oculo-Facial Syndrome in Causing Eye Effects in ZebrafishI Balikova, K Devriendt, J-P Fryns, et al.
The Journal of Thoracic and Cardiovascular Surgery|September 13, 2005
Right aortic arch with vascular ring in one monozygotic twinA Sondakh, W Daenen, M Gewillig, et al.
Clinical Dysmorphology|August 24, 1999
Occipital Horn syndrome in a 2-year-old boyA De Paepe, B Loeys, K Devriendt, et al.
Clinical Genetics|March 25, 2000
The Haspeslagh syndrome (MIM 177980) is caused by an unbalanced reciprocal 6q/9p translocationK Devriendt, M Holvoet, A De Mûelenaere, et al.
Genetic Counseling (Geneva, Switzerland)|May 23, 2002
Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patientT Lukusa, G Van Buggenhout, K Devriendt, et al.
Clinical Genetics|November 15, 2002
Ring syndrome caused by ring chromosome 7 without loss of subtelomeric sequencesJ R Vermeesch, E Baten, J-P Fryns, et al.
The Journal of Pediatrics|August 10, 2000
Deletion of NKX2.1 gene encoding thyroid transcription factor-1 in two siblings with hypothyroidism and respiratory failureN Iwatani, H Mabe, K Devriendt, et al.
Developmental Medicine and Child Neurology|October 1, 1996
Cerebellar hypoplasia in a patient with velo-cardio-facial syndromeK Devriendt, M N Thienen, A Swillen, et al.
Pageof 23

Showing results (41-50 of 230) with videos related to

Sort By:
Pageof 23
American Journal of Medical Genetics|April 11, 2000
Dicentric chromosome 9 due to tandem duplication of the 9p11-q13 region: unusual chromosome 9 variantT Lukusa, K Devriendt, M Holvoet, et al.
Clinical Genetics|January 1, 1996
Alopecia-mental retardation syndrome associated with convulsions and hypergonadotropic hypogonadismK Devriendt, H Van den Berghe, J P Fryns
Molecular Syndromology|December 6, 2011
FOXD1 Duplication Causes Branchial Defects and Interacts with the TFAP2A Gene Implicated in the Branchio-Oculo-Facial Syndrome in Causing Eye Effects in ZebrafishI Balikova, K Devriendt, J-P Fryns, et al.
The Journal of Thoracic and Cardiovascular Surgery|September 13, 2005
Right aortic arch with vascular ring in one monozygotic twinA Sondakh, W Daenen, M Gewillig, et al.
Clinical Dysmorphology|August 24, 1999
Occipital Horn syndrome in a 2-year-old boyA De Paepe, B Loeys, K Devriendt, et al.
Clinical Genetics|March 25, 2000
The Haspeslagh syndrome (MIM 177980) is caused by an unbalanced reciprocal 6q/9p translocationK Devriendt, M Holvoet, A De Mûelenaere, et al.
Genetic Counseling (Geneva, Switzerland)|May 23, 2002
Pericentric inversion with partial 7(q35-->qter) duplication and 7pter deletion: diagnosis by cytogenetic and fish analysis in a 29-year-old male patientT Lukusa, G Van Buggenhout, K Devriendt, et al.
Clinical Genetics|November 15, 2002
Ring syndrome caused by ring chromosome 7 without loss of subtelomeric sequencesJ R Vermeesch, E Baten, J-P Fryns, et al.
The Journal of Pediatrics|August 10, 2000
Deletion of NKX2.1 gene encoding thyroid transcription factor-1 in two siblings with hypothyroidism and respiratory failureN Iwatani, H Mabe, K Devriendt, et al.
Developmental Medicine and Child Neurology|October 1, 1996
Cerebellar hypoplasia in a patient with velo-cardio-facial syndromeK Devriendt, M N Thienen, A Swillen, et al.
Pageof 23