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G Matthijs

Showing results (41-50 of 157) with videos related to

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Journal of Medical Genetics|April 16, 1999
Triplication of distal chromosome 10qK Devriendt, G Matthijs, M Holvoet, et al.
Genetic Counseling (Geneva, Switzerland)|April 23, 2005
Medullary thyroid carcinoma in a child with a new RET mutation and a RET polymorphismK Vandenbosch, M Renard, A Uyttebroeck, et al.
The American Journal of Physiology|September 1, 1989
Erythromycin is a motilin receptor agonistT Peeters, G Matthijs, I Depoortere, et al.
American Journal of Human Genetics|April 29, 1998
Lack of homozygotes for the most frequent disease allele in carbohydrate-deficient glycoprotein syndrome type 1AG Matthijs, E Schollen, E Van Schaftingen, et al.
European Journal of Medical Genetics|August 2, 2005
CDG-Id caused by homozygosity for an ALG3 mutation due to segmental maternal isodisomy UPD3(q21.3-qter)E Schollen, S Grünewald, L Keldermans, et al.
American Journal of Medical Genetics. Part A|July 21, 2004
A novel MSX1 mutation in hypodontiaS De Muynck, E Schollen, G Matthijs, et al.
American Journal of Human Genetics|November 9, 2000
Primary autosomal recessive microcephaly: MCPH5 maps to 1q25-q32C R Jamieson, J P Fryns, J Jacobs, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Carbohydrate-deficient glycoprotein syndrome: beyond the screenJ M Fletcher, G Matthijs, J Jaeken, et al.
Journal of Medical Genetics|February 5, 2002
Okihiro syndrome and acro-renal-ocular syndrome: clinical overlap, expansion of the phenotype, and absence of PAX2 mutations in two new familiesK Becker, P L Beales, D M Calver, et al.
Biochemical and Biophysical Research Communications|April 30, 1992
Structure of the human alpha-2 macroglobulin gene and its promotorG Matthijs, K Devriendt, J J Cassiman, et al.
Pageof 16

Showing results (41-50 of 157) with videos related to

Sort By:
Pageof 16
Journal of Medical Genetics|April 16, 1999
Triplication of distal chromosome 10qK Devriendt, G Matthijs, M Holvoet, et al.
Genetic Counseling (Geneva, Switzerland)|April 23, 2005
Medullary thyroid carcinoma in a child with a new RET mutation and a RET polymorphismK Vandenbosch, M Renard, A Uyttebroeck, et al.
The American Journal of Physiology|September 1, 1989
Erythromycin is a motilin receptor agonistT Peeters, G Matthijs, I Depoortere, et al.
American Journal of Human Genetics|April 29, 1998
Lack of homozygotes for the most frequent disease allele in carbohydrate-deficient glycoprotein syndrome type 1AG Matthijs, E Schollen, E Van Schaftingen, et al.
European Journal of Medical Genetics|August 2, 2005
CDG-Id caused by homozygosity for an ALG3 mutation due to segmental maternal isodisomy UPD3(q21.3-qter)E Schollen, S Grünewald, L Keldermans, et al.
American Journal of Medical Genetics. Part A|July 21, 2004
A novel MSX1 mutation in hypodontiaS De Muynck, E Schollen, G Matthijs, et al.
American Journal of Human Genetics|November 9, 2000
Primary autosomal recessive microcephaly: MCPH5 maps to 1q25-q32C R Jamieson, J P Fryns, J Jacobs, et al.
Journal of Inherited Metabolic Disease|July 15, 2000
Carbohydrate-deficient glycoprotein syndrome: beyond the screenJ M Fletcher, G Matthijs, J Jaeken, et al.
Journal of Medical Genetics|February 5, 2002
Okihiro syndrome and acro-renal-ocular syndrome: clinical overlap, expansion of the phenotype, and absence of PAX2 mutations in two new familiesK Becker, P L Beales, D M Calver, et al.
Biochemical and Biophysical Research Communications|April 30, 1992
Structure of the human alpha-2 macroglobulin gene and its promotorG Matthijs, K Devriendt, J J Cassiman, et al.
Pageof 16