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

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Genetic Counseling (Geneva, Switzerland)|January 1, 1992

Tetraphocomelia and bilateral femorotibial synostosis. A severe variant of the thrombocytopenia-absent radii (TAR) syndrome?J Delooz, P Moerman, K Van den Berghe, et al.

American Journal of Medical Genetics|October 1, 1988

Holzgreve-Wagner-Rehder syndrome: Potter sequence associated with persistent buccopharyngeal membrane. A second observationE Legius, P Moerman, J P Fryns, et al.

Annales De Genetique|January 1, 1984

Cystic hygroma and multiple pterygium syndromeJ P Fryns, K Vandenberghe, P Moerman, et al.

Annales De Genetique|January 1, 1986

Reciprocal translocations and full trisomy (trisomy 18 and trisomy 21) in the offspringJ P Fryns, A Kleczkowska, P Moerman, et al.

Neuropediatrics|April 1, 1997

The effect of behavioural states on cerebral oxygenation during endotracheal suctioning of preterm babiesG Bernert, K von Siebenthal, R Seidl, 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|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 (81-90 of 1,050) with videos related to

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Pageof 105

Genetic Counseling (Geneva, Switzerland)|January 1, 1992

Tetraphocomelia and bilateral femorotibial synostosis. A severe variant of the thrombocytopenia-absent radii (TAR) syndrome?J Delooz, P Moerman, K Van den Berghe, et al.

American Journal of Medical Genetics|October 1, 1988

Holzgreve-Wagner-Rehder syndrome: Potter sequence associated with persistent buccopharyngeal membrane. A second observationE Legius, P Moerman, J P Fryns, et al.

Annales De Genetique|January 1, 1984

Cystic hygroma and multiple pterygium syndromeJ P Fryns, K Vandenberghe, P Moerman, et al.

Annales De Genetique|January 1, 1986

Reciprocal translocations and full trisomy (trisomy 18 and trisomy 21) in the offspringJ P Fryns, A Kleczkowska, P Moerman, et al.

Neuropediatrics|April 1, 1997

The effect of behavioural states on cerebral oxygenation during endotracheal suctioning of preterm babiesG Bernert, K von Siebenthal, R Seidl, 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|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 105