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

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American Journal of Medical Genetics|December 26, 2001

Bilateral tibial agenesis with ectrodactyly (OMIM 119100): further evidence for autosomal recessive inheritanceI Witters, K Devriendt, P Moerman, et al.

Genetic Counseling (Geneva, Switzerland)|January 23, 1999

Skin pigment anomalies and mosaicism for a double autosomal trisomy (48,XX,+18,+20)K Devriendt, G Matthijs, J Meireleire, et al.

Genetic Counseling (Geneva, Switzerland)|April 7, 1999

The phenotypic spectrum of the 10p deletion syndrome versus the classical DiGeorge syndromeH Van Esch, P Groenen, J P Fryns, et al.

Acta Oto-Rhino-Laryngologica Belgica|March 21, 2001

Clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experienceG Vantrappen, N Rommel, K Devriendt, et al.

Genetic Counseling (Geneva, Switzerland)|November 15, 2006

Mathematical disabilities in young primary school children with velo-cardio-facial syndromeB De Smedt, A Swillen, K Devriendt, et al.

Journal of Medical Genetics|June 1, 1997

Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFSA Swillen, K Devriendt, E Legius, et al.

American Journal of Medical Genetics|October 28, 1997

A recognisable behavioural phenotype associated with terminal deletions of the short arm of chromosome 8I Claeys, M Holvoet, B Eyskens, et al.

Genomics|May 23, 1998

Rearrangement of the human CDC5L gene by a t(6;19)(p21;q13.1) in a patient with multicystic renal dysplasiaP M Groenen, G Vanderlinden, K Devriendt, et al.

Genetic Counseling (Geneva, Switzerland)|January 23, 1999

The macrocephaly-cutis marmorata telangiectatica congenita syndrome. Long-term follow-up data in 4 children and adolescentsA Vogels, K Devriendt, E Legius, et al.

American Journal of Medical Genetics|January 25, 2002

MCA syndrome with renal-hepatic-pancreatic dysplasia, posterior fossa cyst, symmetrical limb deficiencies, cleft palate, cardiac and Müllerian duct anomaliesI Witters, K Devriendt, D Spinnewijn, et al.

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Showing results (51-60 of 899) with videos related to

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Pageof 90

American Journal of Medical Genetics|December 26, 2001

Bilateral tibial agenesis with ectrodactyly (OMIM 119100): further evidence for autosomal recessive inheritanceI Witters, K Devriendt, P Moerman, et al.

Genetic Counseling (Geneva, Switzerland)|January 23, 1999

Skin pigment anomalies and mosaicism for a double autosomal trisomy (48,XX,+18,+20)K Devriendt, G Matthijs, J Meireleire, et al.

Genetic Counseling (Geneva, Switzerland)|April 7, 1999

The phenotypic spectrum of the 10p deletion syndrome versus the classical DiGeorge syndromeH Van Esch, P Groenen, J P Fryns, et al.

Acta Oto-Rhino-Laryngologica Belgica|March 21, 2001

Clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experienceG Vantrappen, N Rommel, K Devriendt, et al.

Genetic Counseling (Geneva, Switzerland)|November 15, 2006

Mathematical disabilities in young primary school children with velo-cardio-facial syndromeB De Smedt, A Swillen, K Devriendt, et al.

Journal of Medical Genetics|June 1, 1997

Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 37 children and adolescents with VCFSA Swillen, K Devriendt, E Legius, et al.

American Journal of Medical Genetics|October 28, 1997

A recognisable behavioural phenotype associated with terminal deletions of the short arm of chromosome 8I Claeys, M Holvoet, B Eyskens, et al.

Genomics|May 23, 1998

Rearrangement of the human CDC5L gene by a t(6;19)(p21;q13.1) in a patient with multicystic renal dysplasiaP M Groenen, G Vanderlinden, K Devriendt, et al.

Genetic Counseling (Geneva, Switzerland)|January 23, 1999

The macrocephaly-cutis marmorata telangiectatica congenita syndrome. Long-term follow-up data in 4 children and adolescentsA Vogels, K Devriendt, E Legius, et al.

American Journal of Medical Genetics|January 25, 2002

MCA syndrome with renal-hepatic-pancreatic dysplasia, posterior fossa cyst, symmetrical limb deficiencies, cleft palate, cardiac and Müllerian duct anomaliesI Witters, K Devriendt, D Spinnewijn, et al.

Pageof 90