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K Devriendt

Showing results (61-70 of 230) with videos related to

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Journal of Medical Genetics|January 15, 2003
Chromosome 15 maternal uniparental disomy and psychosis in Prader-Willi syndromeA Vogels, G Matthijs, E Legius, et al.
American Journal of Medical Genetics. Part A|May 16, 2003
Melorheostosis in a family with autosomal dominant osteopoikilosis: report of a third familyPhilippe Debeer, E Pykels, J Lammens, et al.
American Journal of Human Genetics|June 17, 2000
Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinaseA Irrthum, M J Karkkainen, K Devriendt, et al.
Prenatal Diagnosis|May 1, 1996
Elevated maternal serum and amniotic fluid alpha-fetoprotein levels in the Denys-Drash syndromeK Devriendt, K van den Berghe, P Moerman, et al.
American Journal of Medical Genetics|January 23, 1999
Heterogeneity in omphalocoele with absent radial ray complexK Devriendt, J P Fryns, P Moerman, et al.
Journal of Medical Genetics|June 27, 1998
Oto-onycho-peroneal syndrome: confirmation of a syndromeK Devriendt, D Stoffelen, R Pfeiffer, et al.
Genetic Counseling (Geneva, Switzerland)|January 23, 1999
Terminal deletion of chromosome 10q26: delineation of two clinical phenotypesP Petit, K Devriendt, M Azou, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
DiGeorge syndrome and unilateral symbrachydactylyK Devriendt, L De Smet, K De Boeck, et al.
Biochimica Et Biophysica Acta|January 17, 1991
Primary structure of pregnancy zone protein. Molecular cloning of a full-length PZP cDNA clone by the polymerase chain reactionK Devriendt, H Van den Berghe, J J Cassiman, et al.
Journal of Medical Genetics|April 16, 1999
Triplication of distal chromosome 10qK Devriendt, G Matthijs, M Holvoet, et al.
Pageof 23

Showing results (61-70 of 230) with videos related to

Sort By:
Pageof 23
Journal of Medical Genetics|January 15, 2003
Chromosome 15 maternal uniparental disomy and psychosis in Prader-Willi syndromeA Vogels, G Matthijs, E Legius, et al.
American Journal of Medical Genetics. Part A|May 16, 2003
Melorheostosis in a family with autosomal dominant osteopoikilosis: report of a third familyPhilippe Debeer, E Pykels, J Lammens, et al.
American Journal of Human Genetics|June 17, 2000
Congenital hereditary lymphedema caused by a mutation that inactivates VEGFR3 tyrosine kinaseA Irrthum, M J Karkkainen, K Devriendt, et al.
Prenatal Diagnosis|May 1, 1996
Elevated maternal serum and amniotic fluid alpha-fetoprotein levels in the Denys-Drash syndromeK Devriendt, K van den Berghe, P Moerman, et al.
American Journal of Medical Genetics|January 23, 1999
Heterogeneity in omphalocoele with absent radial ray complexK Devriendt, J P Fryns, P Moerman, et al.
Journal of Medical Genetics|June 27, 1998
Oto-onycho-peroneal syndrome: confirmation of a syndromeK Devriendt, D Stoffelen, R Pfeiffer, et al.
Genetic Counseling (Geneva, Switzerland)|January 23, 1999
Terminal deletion of chromosome 10q26: delineation of two clinical phenotypesP Petit, K Devriendt, M Azou, et al.
Genetic Counseling (Geneva, Switzerland)|January 1, 1997
DiGeorge syndrome and unilateral symbrachydactylyK Devriendt, L De Smet, K De Boeck, et al.
Biochimica Et Biophysica Acta|January 17, 1991
Primary structure of pregnancy zone protein. Molecular cloning of a full-length PZP cDNA clone by the polymerase chain reactionK Devriendt, H Van den Berghe, J J Cassiman, et al.
Journal of Medical Genetics|April 16, 1999
Triplication of distal chromosome 10qK Devriendt, G Matthijs, M Holvoet, et al.
Pageof 23