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J Halley

Showing results (171-180 of 194) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 27, 2015
The expanding phenotype of COL4A1 and COL4A2 mutations: clinical data on 13 newly identified families and a review of the literatureMarije E C Meuwissen, Dicky J J Halley, Liesbeth S Smit, et al.
Ecology and Evolution|January 24, 2014
Antiparasite treatments reduce humoral immunity and impact oxidative status in raptor nestlingsSveinn Are Hanssen, Jan Ove Bustnes, Lisbeth Schnug, et al.
Epilepsia|March 11, 2004
Evidence for linkage between juvenile myoclonic epilepsy-related idiopathic generalized epilepsy and 6p11-12 in Dutch familiesDalila Pinto, Gerrit-Jan de Haan, Guus A M A J Janssen, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 24, 2017
Development and Function of Immune Cells in an Adolescent Patient With a Deficiency in the Interleukin-10 ReceptorSharon Veenbergen, Marieke A van Leeuwen, Gertjan J Driessen, et al.
Journal of Medical Genetics|January 1, 1996
Identification of a nonsense mutation at the 5' end of the TSC2 gene in a family with a presumptive diagnosis of tuberous sclerosis complexR Vrtel, S Verhoef, K Bouman, et al.
Human Molecular Genetics|January 15, 1999
The spectrum of mutations in UBE3A causing Angelman syndromeP Fang, E Lev-Lehman, T F Tsai, et al.
Epilepsia|August 27, 2004
Univerricht-Lundborg disease: underdiagnosed in the NetherlandsGerrit-Jan de Haan, Dicky J J Halley, Jan C Doelman, et al.
Ecotoxicology and Environmental Safety|March 27, 2012
Blood plasma clinical-chemical parameters as biomarker endpoints for organohalogen contaminant exposure in Norwegian raptor nestlingsChristian Sonne, Jan O Bustnes, Dorte Herzke, et al.
European Journal of Cancer (Oxford, England : 1990)|October 13, 2001
Large regional differences in the frequency of distinct BRCA1/BRCA2 mutations in 517 Dutch breast and/or ovarian cancer familiesL C Verhoog, A M van den Ouweland, E Berns, et al.
European Journal of Human Genetics : EJHG|February 16, 2012
COL4A2 mutation associated with familial porencephaly and small-vessel diseaseElly Verbeek, Marije E C Meuwissen, Frans W Verheijen, et al.
Pageof 20

Showing results (171-180 of 194) with videos related to

Sort By:
Pageof 20
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 27, 2015
The expanding phenotype of COL4A1 and COL4A2 mutations: clinical data on 13 newly identified families and a review of the literatureMarije E C Meuwissen, Dicky J J Halley, Liesbeth S Smit, et al.
Ecology and Evolution|January 24, 2014
Antiparasite treatments reduce humoral immunity and impact oxidative status in raptor nestlingsSveinn Are Hanssen, Jan Ove Bustnes, Lisbeth Schnug, et al.
Epilepsia|March 11, 2004
Evidence for linkage between juvenile myoclonic epilepsy-related idiopathic generalized epilepsy and 6p11-12 in Dutch familiesDalila Pinto, Gerrit-Jan de Haan, Guus A M A J Janssen, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 24, 2017
Development and Function of Immune Cells in an Adolescent Patient With a Deficiency in the Interleukin-10 ReceptorSharon Veenbergen, Marieke A van Leeuwen, Gertjan J Driessen, et al.
Journal of Medical Genetics|January 1, 1996
Identification of a nonsense mutation at the 5' end of the TSC2 gene in a family with a presumptive diagnosis of tuberous sclerosis complexR Vrtel, S Verhoef, K Bouman, et al.
Human Molecular Genetics|January 15, 1999
The spectrum of mutations in UBE3A causing Angelman syndromeP Fang, E Lev-Lehman, T F Tsai, et al.
Epilepsia|August 27, 2004
Univerricht-Lundborg disease: underdiagnosed in the NetherlandsGerrit-Jan de Haan, Dicky J J Halley, Jan C Doelman, et al.
Ecotoxicology and Environmental Safety|March 27, 2012
Blood plasma clinical-chemical parameters as biomarker endpoints for organohalogen contaminant exposure in Norwegian raptor nestlingsChristian Sonne, Jan O Bustnes, Dorte Herzke, et al.
European Journal of Cancer (Oxford, England : 1990)|October 13, 2001
Large regional differences in the frequency of distinct BRCA1/BRCA2 mutations in 517 Dutch breast and/or ovarian cancer familiesL C Verhoog, A M van den Ouweland, E Berns, et al.
European Journal of Human Genetics : EJHG|February 16, 2012
COL4A2 mutation associated with familial porencephaly and small-vessel diseaseElly Verbeek, Marije E C Meuwissen, Frans W Verheijen, et al.
Pageof 20