K Devriendt|P De Cock|J P Fryns - JoVE Visualize

Showing results (11-20 of 899) with videos related to

Pageof 90

Sort By:

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

Annales De Genetique|August 26, 1998

Wolf-Hirschhorn syndrome with cryptic 4p16.3 deletion and balanced/unbalanced mosaicism in the motherJ P Fryns, E Smeets, K Devriendt, et al.

Clinical Dysmorphology|May 18, 1999

Mild dysmorphic signs in two male sibs with partial trisomy 2q32.1-->q35 due to maternal ins(14;2) translocationT Lukusa, K Devriendt, J Jaeken, et al.

American Journal of Medical Genetics|February 17, 2001

Chromosome 22q11 deletion syndrome: update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complicationsA Swillen, A Vogels, K Devriendt, et al.

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

Clinical Genetics|October 27, 1998

Severe mental retardation-distal arthrogryposis in the upper limbs and complex chromosomal rearrangements resulting from a 10q25-->qter deletionT Lukusa, K Devriendt, M Holvoet, et al.

Genetic Counseling (Geneva, Switzerland)|February 12, 2002

Children with a 22q11 deletion versus children with a speech-language impairment and learning disability: behavior during primary school ageA Swillen, K Devriendt, P Ghesquière, et al.

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.

Pageof 90

Showing results (11-20 of 899) with videos related to

Sort By:

Pageof 90

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

Annales De Genetique|August 26, 1998

Wolf-Hirschhorn syndrome with cryptic 4p16.3 deletion and balanced/unbalanced mosaicism in the motherJ P Fryns, E Smeets, K Devriendt, et al.

Clinical Dysmorphology|May 18, 1999

Mild dysmorphic signs in two male sibs with partial trisomy 2q32.1-->q35 due to maternal ins(14;2) translocationT Lukusa, K Devriendt, J Jaeken, et al.

American Journal of Medical Genetics|February 17, 2001

Chromosome 22q11 deletion syndrome: update and review of the clinical features, cognitive-behavioral spectrum, and psychiatric complicationsA Swillen, A Vogels, K Devriendt, et al.

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

Clinical Genetics|October 27, 1998

Severe mental retardation-distal arthrogryposis in the upper limbs and complex chromosomal rearrangements resulting from a 10q25-->qter deletionT Lukusa, K Devriendt, M Holvoet, et al.

Genetic Counseling (Geneva, Switzerland)|February 12, 2002

Children with a 22q11 deletion versus children with a speech-language impairment and learning disability: behavior during primary school ageA Swillen, K Devriendt, P Ghesquière, et al.

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.

Pageof 90