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P De Cock

Showing results (31-40 of 66) with videos related to

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Biophysik|January 1, 1972
Metabolism of deoxycytidine in isolated perfused organsG B Gerber, B Zicha, J Deroo, et al.
BMC Pregnancy and Childbirth|October 15, 2015
Exclusive breastfeeding after home versus hospital birth in primary midwifery care in the NetherlandsT P de Cock, J Manniën, C Geerts, et al.
Archives of Disease in Childhood|August 1, 1994
Carbohydrate deficient glycoprotein syndrome type II: a deficiency in Golgi localised N-acetyl-glucosaminyltransferase IIJ Jaeken, H Schachter, H Carchon, et al.
Annales De Genetique|January 1, 1995
Terminal deletion in chromosome region 8p23.1-8pter in a child with features of velo-cardio-facial syndromeK Devriendt, K De Mars, P De Cock, et al.
Annales De Genetique|January 1, 1980
De novo paracentric inversion in a microcephalic boy: 46,XY, inv(14)(q13q24)J Jaeken, J P Fryns, L Standaert, et al.
Human Movement Science|June 18, 2004
Aspects of the validity of the Movement Assessment Battery for ChildrenH Van Waelvelde, W De Weerdt, P De Cock, et al.
Journal of Medical Genetics|March 4, 2008
The facial dysmorphy in the newly recognised microdeletion 2p15-p16.1 refined to a 570 kb region in 2p15E Chabchoub, J R Vermeesch, T de Ravel, et al.
The Central African Journal of Medicine|April 19, 2002
The reliability of the Shona version of the EQ-5DJ Jelsma, K Mhundwa, W De Weerdt, et al.
Clinical Genetics|January 1, 1992
Severe pre- and postnatal growth retardation, developmental delay with hypotonia and marked hypotrophy of the distal extremities, dental anomalies, and eczematous skin. A new autosomal recessive entityC Grubben, P de Cock, M Borghgraef, et al.
Genetic Counseling (Geneva, Switzerland)|April 28, 2010
Duplication of the VHL and IRAK2 genes in a patient with mental retardation/multiple congenital anomalies, epilepsy and ectomorphic habitusE Chabchoub, G Michils, J R Vermeesch, et al.
Pageof 7

Showing results (31-40 of 66) with videos related to

Sort By:
Pageof 7
Biophysik|January 1, 1972
Metabolism of deoxycytidine in isolated perfused organsG B Gerber, B Zicha, J Deroo, et al.
BMC Pregnancy and Childbirth|October 15, 2015
Exclusive breastfeeding after home versus hospital birth in primary midwifery care in the NetherlandsT P de Cock, J Manniën, C Geerts, et al.
Archives of Disease in Childhood|August 1, 1994
Carbohydrate deficient glycoprotein syndrome type II: a deficiency in Golgi localised N-acetyl-glucosaminyltransferase IIJ Jaeken, H Schachter, H Carchon, et al.
Annales De Genetique|January 1, 1995
Terminal deletion in chromosome region 8p23.1-8pter in a child with features of velo-cardio-facial syndromeK Devriendt, K De Mars, P De Cock, et al.
Annales De Genetique|January 1, 1980
De novo paracentric inversion in a microcephalic boy: 46,XY, inv(14)(q13q24)J Jaeken, J P Fryns, L Standaert, et al.
Human Movement Science|June 18, 2004
Aspects of the validity of the Movement Assessment Battery for ChildrenH Van Waelvelde, W De Weerdt, P De Cock, et al.
Journal of Medical Genetics|March 4, 2008
The facial dysmorphy in the newly recognised microdeletion 2p15-p16.1 refined to a 570 kb region in 2p15E Chabchoub, J R Vermeesch, T de Ravel, et al.
The Central African Journal of Medicine|April 19, 2002
The reliability of the Shona version of the EQ-5DJ Jelsma, K Mhundwa, W De Weerdt, et al.
Clinical Genetics|January 1, 1992
Severe pre- and postnatal growth retardation, developmental delay with hypotonia and marked hypotrophy of the distal extremities, dental anomalies, and eczematous skin. A new autosomal recessive entityC Grubben, P de Cock, M Borghgraef, et al.
Genetic Counseling (Geneva, Switzerland)|April 28, 2010
Duplication of the VHL and IRAK2 genes in a patient with mental retardation/multiple congenital anomalies, epilepsy and ectomorphic habitusE Chabchoub, G Michils, J R Vermeesch, et al.
Pageof 7