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K Devriendt

Showing results (101-110 of 230) with videos related to

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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.
American Journal of Medical Genetics|July 13, 2002
Resolution of non-immune hydrops in Noonan syndrome with favorable outcomeI Witters, B Spitz, C Van Hole, et al.
Acta Oto-Rhino-Laryngologica Belgica|July 3, 2003
Velo-cardio-facial syndrome: guidelines for diagnosis, treatment and follow-up of ent manifestationsG Vantrappen, N Rommel, A Swillen, et al.
The Journal of Clinical Investigation|April 1, 1995
Severe alport phenotype in a woman with two missense mutations in the same COL4A5 gene and preponderant inactivation of the X chromosome carrying the normal alleleC Guo, B Van Damme, Y Vanrenterghem, et al.
Neuropsychologia|October 20, 2006
Mathematical disabilities in children with velo-cardio-facial syndromeB De Smedt, A Swillen, K Devriendt, et al.
Journal of Intellectual Disability Research : JIDR|September 12, 2007
Intellectual abilities in a large sample of children with Velo-Cardio-Facial Syndrome: an updateB De Smedt, K Devriendt, J-P Fryns, et al.
Clinical Dysmorphology|May 29, 2000
Severe short stature, hyperphalangy of the index fingers, mental retardation and facial dysmorphismK Devriendt, K Keymolen, L Roelen, et al.
Human Genetics|June 1, 1997
Interstitial telomeric sequences at the junction site of a jumping translocationJ R Vermeesch, P Petit, F Speleman, et al.
Prenatal Diagnosis|March 4, 1998
Prenatal diagnosis of a terminal short arm deletion of chromosome 8 in a fetus with an atrioventricular septal defectK Devriendt, D Van Schoubroeck, B Eyskens, et al.
American Journal of Medical Genetics|December 26, 2001
Bilateral tibial agenesis with ectrodactyly (OMIM 119100): further evidence for autosomal recessive inheritanceI Witters, K Devriendt, P Moerman, et al.
Pageof 23

Showing results (101-110 of 230) with videos related to

Sort By:
Pageof 23
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.
American Journal of Medical Genetics|July 13, 2002
Resolution of non-immune hydrops in Noonan syndrome with favorable outcomeI Witters, B Spitz, C Van Hole, et al.
Acta Oto-Rhino-Laryngologica Belgica|July 3, 2003
Velo-cardio-facial syndrome: guidelines for diagnosis, treatment and follow-up of ent manifestationsG Vantrappen, N Rommel, A Swillen, et al.
The Journal of Clinical Investigation|April 1, 1995
Severe alport phenotype in a woman with two missense mutations in the same COL4A5 gene and preponderant inactivation of the X chromosome carrying the normal alleleC Guo, B Van Damme, Y Vanrenterghem, et al.
Neuropsychologia|October 20, 2006
Mathematical disabilities in children with velo-cardio-facial syndromeB De Smedt, A Swillen, K Devriendt, et al.
Journal of Intellectual Disability Research : JIDR|September 12, 2007
Intellectual abilities in a large sample of children with Velo-Cardio-Facial Syndrome: an updateB De Smedt, K Devriendt, J-P Fryns, et al.
Clinical Dysmorphology|May 29, 2000
Severe short stature, hyperphalangy of the index fingers, mental retardation and facial dysmorphismK Devriendt, K Keymolen, L Roelen, et al.
Human Genetics|June 1, 1997
Interstitial telomeric sequences at the junction site of a jumping translocationJ R Vermeesch, P Petit, F Speleman, et al.
Prenatal Diagnosis|March 4, 1998
Prenatal diagnosis of a terminal short arm deletion of chromosome 8 in a fetus with an atrioventricular septal defectK Devriendt, D Van Schoubroeck, B Eyskens, et al.
American Journal of Medical Genetics|December 26, 2001
Bilateral tibial agenesis with ectrodactyly (OMIM 119100): further evidence for autosomal recessive inheritanceI Witters, K Devriendt, P Moerman, et al.
Pageof 23