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K Devriendt

Showing results (111-120 of 230) with videos related to

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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)|February 26, 2009
Lobar holoprosencephaly in 18pter deletion resulting from the karyotype 45,X,-18,der(8;18)t(8; 18)(pter;p11.21)I Witters, I Balikova, M Cannie, 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.
Human Genetics|May 31, 2001
Identification of novel DKC1 mutations in patients with dyskeratosis congenita: implications for pathophysiology and diagnosisS W Knight, T J Vulliamy, B Morgan, et al.
Gene|November 15, 2001
PALML, a novel paralemmin-related gene mapping on human chromosome 1p21N Andreu, M Escarceller, S Feather, 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.
Pageof 23

Showing results (111-120 of 230) with videos related to

Sort By:
Pageof 23
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)|February 26, 2009
Lobar holoprosencephaly in 18pter deletion resulting from the karyotype 45,X,-18,der(8;18)t(8; 18)(pter;p11.21)I Witters, I Balikova, M Cannie, 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.
Human Genetics|May 31, 2001
Identification of novel DKC1 mutations in patients with dyskeratosis congenita: implications for pathophysiology and diagnosisS W Knight, T J Vulliamy, B Morgan, et al.
Gene|November 15, 2001
PALML, a novel paralemmin-related gene mapping on human chromosome 1p21N Andreu, M Escarceller, S Feather, 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.
Pageof 23