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

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Journal of Medical Genetics|April 16, 1999

Triplication of distal chromosome 10qK Devriendt, G Matthijs, M Holvoet, et al.

Annales De Genetique|January 1, 1980

De novo paracentric inversion in a microcephalic boy: 46,XY, inv(14)(q13q24)J Jaeken, J P Fryns, L Standaert, et al.

Clinical Genetics|January 1, 1992

Severe pre- and postnatal growth retardation, developmental delay with hypotonia and marked hypotrophy of the distal extremities, dental anomalies, and eczematous skin. A new autosomal recessive entityC Grubben, P de Cock, M Borghgraef, et al.

Genetic Counseling (Geneva, Switzerland)|May 3, 2003

Pre-academic and early academic achievement in children with velocardiofacial syndrome (del22q11.2) of borderline or normal intelligenceB De Smedt, A Swillen, P Ghesquière, et al.

Genetic Counseling (Geneva, Switzerland)|July 23, 2003

Partial monosomy 11q and trisomy 12q: variable expression in two siblingsT Lukusa, M Holvoet, J R Vermeesch, et al.

Genetic Counseling (Geneva, Switzerland)|November 3, 2004

Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorderT Lukusa, J R Vermeesch, M Holvoet, et al.

Genetic Counseling (Geneva, Switzerland)|October 20, 1998

Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p)P Petit, K Devriendt, J R Vermeesch, et al.

Journal of Medical Genetics|February 25, 1998

Proteinuria in a patient with the diaphragmatic hernia-hypertelorism-myopia-deafness syndrome: further evidence that the facio-oculo-acoustico-renal syndrome represents the same entityK Devriendt, L Standaert, C Van Hole, et al.

Journal of Medical Genetics|May 1, 1997

Chromosome 22q11 deletion presenting as the Potter sequenceK Devriendt, P Moerman, D Van Schoubroeck, et al.

Journal of Medical Genetics|May 23, 1998

Two adult females with a distinct familial mental retardation syndrome: non-progressive neurological symptoms with ataxia and hypotonia, similar facial appearance, hypergonadotrophic hypogonadism, and retinal dystrophyJ P Fryns, C Van Lingen, K Devriendt, et al.

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Showing results (31-40 of 899) with videos related to

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Pageof 90

Journal of Medical Genetics|April 16, 1999

Triplication of distal chromosome 10qK Devriendt, G Matthijs, M Holvoet, et al.

Annales De Genetique|January 1, 1980

De novo paracentric inversion in a microcephalic boy: 46,XY, inv(14)(q13q24)J Jaeken, J P Fryns, L Standaert, et al.

Clinical Genetics|January 1, 1992

Severe pre- and postnatal growth retardation, developmental delay with hypotonia and marked hypotrophy of the distal extremities, dental anomalies, and eczematous skin. A new autosomal recessive entityC Grubben, P de Cock, M Borghgraef, et al.

Genetic Counseling (Geneva, Switzerland)|May 3, 2003

Pre-academic and early academic achievement in children with velocardiofacial syndrome (del22q11.2) of borderline or normal intelligenceB De Smedt, A Swillen, P Ghesquière, et al.

Genetic Counseling (Geneva, Switzerland)|July 23, 2003

Partial monosomy 11q and trisomy 12q: variable expression in two siblingsT Lukusa, M Holvoet, J R Vermeesch, et al.

Genetic Counseling (Geneva, Switzerland)|November 3, 2004

Deletion 2q37.3 and autism: molecular cytogenetic mapping of the candidate region for autistic disorderT Lukusa, J R Vermeesch, M Holvoet, et al.

Genetic Counseling (Geneva, Switzerland)|October 20, 1998

Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p)P Petit, K Devriendt, J R Vermeesch, et al.

Journal of Medical Genetics|February 25, 1998

Proteinuria in a patient with the diaphragmatic hernia-hypertelorism-myopia-deafness syndrome: further evidence that the facio-oculo-acoustico-renal syndrome represents the same entityK Devriendt, L Standaert, C Van Hole, et al.

Journal of Medical Genetics|May 1, 1997

Chromosome 22q11 deletion presenting as the Potter sequenceK Devriendt, P Moerman, D Van Schoubroeck, et al.

Journal of Medical Genetics|May 23, 1998

Two adult females with a distinct familial mental retardation syndrome: non-progressive neurological symptoms with ataxia and hypotonia, similar facial appearance, hypergonadotrophic hypogonadism, and retinal dystrophyJ P Fryns, C Van Lingen, K Devriendt, et al.

Pageof 90