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K Devriendt

Showing results (121-130 of 230) with videos related to

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Genetic Counseling (Geneva, Switzerland)|January 23, 1999
The macrocephaly-cutis marmorata telangiectatica congenita syndrome. Long-term follow-up data in 4 children and adolescentsA Vogels, K Devriendt, E Legius, et al.
American Journal of Medical Genetics|January 25, 2002
MCA syndrome with renal-hepatic-pancreatic dysplasia, posterior fossa cyst, symmetrical limb deficiencies, cleft palate, cardiac and Müllerian duct anomaliesI Witters, K Devriendt, D Spinnewijn, et al.
Clinical Genetics|January 4, 2012
Aarskog-Scott syndrome: first report of a duplication in the FGD1 geneN Ronce, I Maystadt, C Hubert, et al.
Genetic Counseling (Geneva, Switzerland)|April 7, 1999
The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescenceA Swillen, K Devriendt, E Legius, et al.
European Journal of Medical Genetics|May 24, 2014
Exome sequencing identifies a recessive PIGN splice site mutation as a cause of syndromic congenital diaphragmatic herniaP D Brady, Philippe Moerman, Luc De Catte, et al.
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|August 5, 2000
Neuropsychological, learning and psychosocial profile of primary school aged children with the velo-cardio-facial syndrome (22q11 deletion): evidence for a nonverbal learning disability?A Swillen, L Vandeputte, J Cracco, et al.
The British Journal of Ophthalmology|April 17, 2001
Autosomal dominant microcephaly--lymphoedema-chorioretinal dysplasia syndromeI Casteels, K Devriendt, H Van Cleynenbreugel, et al.
Prenatal Diagnosis|October 15, 2013
Identification of dosage-sensitive genes in fetuses referred with severe isolated congenital diaphragmatic herniaP D Brady, P DeKoninck, J P Fryns, et al.
Journal of Medical Genetics|April 1, 1997
Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysisK Devriendt, G Matthijs, S Claes, et al.
Annales De Genetique|January 1, 1997
Agenesis of corpus callosum and anophthalmia in the asplenia syndrome. A recognisable association?K Devriendt, G Naulaers, G Matthijs, et al.
Pageof 23

Showing results (121-130 of 230) with videos related to

Sort By:
Pageof 23
Genetic Counseling (Geneva, Switzerland)|January 23, 1999
The macrocephaly-cutis marmorata telangiectatica congenita syndrome. Long-term follow-up data in 4 children and adolescentsA Vogels, K Devriendt, E Legius, et al.
American Journal of Medical Genetics|January 25, 2002
MCA syndrome with renal-hepatic-pancreatic dysplasia, posterior fossa cyst, symmetrical limb deficiencies, cleft palate, cardiac and Müllerian duct anomaliesI Witters, K Devriendt, D Spinnewijn, et al.
Clinical Genetics|January 4, 2012
Aarskog-Scott syndrome: first report of a duplication in the FGD1 geneN Ronce, I Maystadt, C Hubert, et al.
Genetic Counseling (Geneva, Switzerland)|April 7, 1999
The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescenceA Swillen, K Devriendt, E Legius, et al.
European Journal of Medical Genetics|May 24, 2014
Exome sequencing identifies a recessive PIGN splice site mutation as a cause of syndromic congenital diaphragmatic herniaP D Brady, Philippe Moerman, Luc De Catte, et al.
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|August 5, 2000
Neuropsychological, learning and psychosocial profile of primary school aged children with the velo-cardio-facial syndrome (22q11 deletion): evidence for a nonverbal learning disability?A Swillen, L Vandeputte, J Cracco, et al.
The British Journal of Ophthalmology|April 17, 2001
Autosomal dominant microcephaly--lymphoedema-chorioretinal dysplasia syndromeI Casteels, K Devriendt, H Van Cleynenbreugel, et al.
Prenatal Diagnosis|October 15, 2013
Identification of dosage-sensitive genes in fetuses referred with severe isolated congenital diaphragmatic herniaP D Brady, P DeKoninck, J P Fryns, et al.
Journal of Medical Genetics|April 1, 1997
Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysisK Devriendt, G Matthijs, S Claes, et al.
Annales De Genetique|January 1, 1997
Agenesis of corpus callosum and anophthalmia in the asplenia syndrome. A recognisable association?K Devriendt, G Naulaers, G Matthijs, et al.
Pageof 23