K Devriendt|J P Fryns|P Moerman|C Vanhole|H Devlieger - JoVE Visualize

Showing results (51-60 of 1,050) with videos related to

Pageof 105

Sort By:

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.

European Journal of Obstetrics, Gynecology, and Reproductive Biology|April 16, 1991

Abdominal distension as the first echographic sign of hydrometrocolpos in a female fetusP Petit, D Thomas, P Moerman, et al.

Genetic Counseling (Geneva, Switzerland)|January 1, 1994

Catel-Manzke palatodigital syndrome in a second trimester female foetus with nuchal oedema, costovertebral anomalies and radial ray defectP Petit, P Moerman, E Legius, et al.

Prenatal Diagnosis|March 4, 1998

Polyhydramnios as a prenatal symptom of the digeorge/velo-cardio-facial syndromeK Devriendt, D Van Schoubroeck, B Eyskens, 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.

Clinical Dysmorphology|August 24, 1999

Occipital Horn syndrome in a 2-year-old boyA De Paepe, B Loeys, K Devriendt, 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.

Pageof 105

Showing results (51-60 of 1,050) with videos related to

Sort By:

Pageof 105

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.

European Journal of Obstetrics, Gynecology, and Reproductive Biology|April 16, 1991

Abdominal distension as the first echographic sign of hydrometrocolpos in a female fetusP Petit, D Thomas, P Moerman, et al.

Genetic Counseling (Geneva, Switzerland)|January 1, 1994

Catel-Manzke palatodigital syndrome in a second trimester female foetus with nuchal oedema, costovertebral anomalies and radial ray defectP Petit, P Moerman, E Legius, et al.

Prenatal Diagnosis|March 4, 1998

Polyhydramnios as a prenatal symptom of the digeorge/velo-cardio-facial syndromeK Devriendt, D Van Schoubroeck, B Eyskens, 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.

Clinical Dysmorphology|August 24, 1999

Occipital Horn syndrome in a 2-year-old boyA De Paepe, B Loeys, K Devriendt, 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.

Pageof 105