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K Devriendt

Showing results (141-150 of 230) with videos related to

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American Journal of Medical Genetics|January 11, 1996
Ichthyosis-characteristic appearance-mental retardation syndrome with distinct histological skin abnormalitiesK Devriendt, J van den Oord, R De Vos, et al.
Gene|September 30, 1989
A cluster of alpha 2-macroglobulin-related genes (alpha 2 M) on human chromosome 12p: cloning of the pregnancy-zone protein gene and an alpha 2M pseudogeneK Devriendt, J Zhang, F van Leuven, et al.
Clinical Genetics|May 1, 1996
Cohen syndrome: the clinical symptoms and stigmata at a young ageJ P Fryns, E Legius, K Devriendt, et al.
American Journal of Medical Genetics. Part A|July 21, 2004
A novel NOG mutation Pro37Arg in a family with tarsal and carpal synostosesP Debeer, J-P Fryns, K Devriendt, et al.
International Journal of Oral and Maxillofacial Surgery|June 21, 2017
Anthropometric and aesthetic outcomes for the nasolabial region in 101 consecutive African children with unilateral cleft lip one year after repair using the anatomical subunit approximation techniqueS Mbuyi-Musanzayi, F Tshilombo Katombe, P Lukusa Tshilobo, et al.
Clinical Genetics|November 15, 2002
Involvement of a palindromic chromosome 22-specific low-copy repeat in a constitutional t(X; 22)(q27;q11)P Debeer, R Mols, C Huysmans, et al.
Journal of Medical Genetics|June 14, 2001
Pregnancy outcome and long term prognosis in 868 children born after second trimester amniocentesis for maternal serum positive triple test screening and normal prenatal karyotypeI Witters, E Legius, K Devriendt, et al.
Prenatal Diagnosis|May 10, 2002
Prenatal findings in a monozygotic twin pregnancy with Costello syndromeT Van den Bosch, D Van Schoubroeck, J P Fryns, et al.
Journal of Medical Genetics|June 7, 2005
Low expression VEGF haplotype increases the risk for tetralogy of Fallot: a family based association studyD Lambrechts, K Devriendt, D A Driscoll, et al.
Journal of Medical Genetics|October 23, 1998
The prevalence of PAX2 mutations in patients with isolated colobomas or colobomas associated with urogenital anomaliesH E Cunliffe, L A McNoe, T A Ward, et al.
Pageof 23

Showing results (141-150 of 230) with videos related to

Sort By:
Pageof 23
American Journal of Medical Genetics|January 11, 1996
Ichthyosis-characteristic appearance-mental retardation syndrome with distinct histological skin abnormalitiesK Devriendt, J van den Oord, R De Vos, et al.
Gene|September 30, 1989
A cluster of alpha 2-macroglobulin-related genes (alpha 2 M) on human chromosome 12p: cloning of the pregnancy-zone protein gene and an alpha 2M pseudogeneK Devriendt, J Zhang, F van Leuven, et al.
Clinical Genetics|May 1, 1996
Cohen syndrome: the clinical symptoms and stigmata at a young ageJ P Fryns, E Legius, K Devriendt, et al.
American Journal of Medical Genetics. Part A|July 21, 2004
A novel NOG mutation Pro37Arg in a family with tarsal and carpal synostosesP Debeer, J-P Fryns, K Devriendt, et al.
International Journal of Oral and Maxillofacial Surgery|June 21, 2017
Anthropometric and aesthetic outcomes for the nasolabial region in 101 consecutive African children with unilateral cleft lip one year after repair using the anatomical subunit approximation techniqueS Mbuyi-Musanzayi, F Tshilombo Katombe, P Lukusa Tshilobo, et al.
Clinical Genetics|November 15, 2002
Involvement of a palindromic chromosome 22-specific low-copy repeat in a constitutional t(X; 22)(q27;q11)P Debeer, R Mols, C Huysmans, et al.
Journal of Medical Genetics|June 14, 2001
Pregnancy outcome and long term prognosis in 868 children born after second trimester amniocentesis for maternal serum positive triple test screening and normal prenatal karyotypeI Witters, E Legius, K Devriendt, et al.
Prenatal Diagnosis|May 10, 2002
Prenatal findings in a monozygotic twin pregnancy with Costello syndromeT Van den Bosch, D Van Schoubroeck, J P Fryns, et al.
Journal of Medical Genetics|June 7, 2005
Low expression VEGF haplotype increases the risk for tetralogy of Fallot: a family based association studyD Lambrechts, K Devriendt, D A Driscoll, et al.
Journal of Medical Genetics|October 23, 1998
The prevalence of PAX2 mutations in patients with isolated colobomas or colobomas associated with urogenital anomaliesH E Cunliffe, L A McNoe, T A Ward, et al.
Pageof 23