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Showing results (321-330 of 391) with videos related to

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Journal of the American Academy of Dermatology|February 6, 2007
From sporadic atypical nevi to familial melanoma: risk analysis for melanoma in sporadic atypical nevus patientsFemke A de Snoo, Marije W Kroon, Wilma Bergman, et al.
Acta Neuropathologica|May 21, 2003
Evaluation of diagnostic NOTCH3 immunostaining in CADASILSaskia A J Lesnik Oberstein, Sjoerd G van Duinen, Rivka van den Boom, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 9, 2001
New mutations in the neuronal ceroid lipofuscinosis genesS E Mole, N A Zhong, A Sarpong, et al.
Human Mutation|January 1, 1997
Deletions spanning the neurofibromatosis type 1 gene: implications for genotype-phenotype correlations in neurofibromatosis type 1?M H Cnossen, M N van der Est, M H Breuning, et al.
The Journal of Clinical Endocrinology and Metabolism|June 22, 2006
Clinical and biochemical characteristics of a male patient with a novel homozygous STAT5b mutationSolrun Vidarsdottir, Marie J E Walenkamp, Alberto M Pereira, et al.
Journal of the American Society of Nephrology : JASN|March 30, 2016
Inhibition of Activin Signaling Slows Progression of Polycystic Kidney DiseaseWouter N Leonhard, Steven J Kunnen, Anna J Plugge, et al.
European Journal of Human Genetics : EJHG|May 14, 2009
A new diagnostic workflow for patients with mental retardation and/or multiple congenital abnormalities: test arrays firstAntoinet C J Gijsbers, Janet Y K Lew, Cathy A J Bosch, et al.
Journal of the American Society of Nephrology : JASN|November 30, 1999
Aberrant splicing in the PKD2 gene as a cause of polycystic kidney diseaseD M Reynolds, T Hayashi, Y Cai, et al.
Cytogenetic and Genome Research|September 29, 2007
Variation of CNV distribution in five different ethnic populationsS J White, L E L M Vissers, A Geurts van Kessel, et al.
Leukemia|February 3, 1998
Detection of CBP rearrangements in acute myelogenous leukemia with t(8;16)R H Giles, J G Dauwerse, C Higgins, et al.
Pageof 40

Showing results (321-330 of 391) with videos related to

Sort By:
Pageof 40
Journal of the American Academy of Dermatology|February 6, 2007
From sporadic atypical nevi to familial melanoma: risk analysis for melanoma in sporadic atypical nevus patientsFemke A de Snoo, Marije W Kroon, Wilma Bergman, et al.
Acta Neuropathologica|May 21, 2003
Evaluation of diagnostic NOTCH3 immunostaining in CADASILSaskia A J Lesnik Oberstein, Sjoerd G van Duinen, Rivka van den Boom, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 9, 2001
New mutations in the neuronal ceroid lipofuscinosis genesS E Mole, N A Zhong, A Sarpong, et al.
Human Mutation|January 1, 1997
Deletions spanning the neurofibromatosis type 1 gene: implications for genotype-phenotype correlations in neurofibromatosis type 1?M H Cnossen, M N van der Est, M H Breuning, et al.
The Journal of Clinical Endocrinology and Metabolism|June 22, 2006
Clinical and biochemical characteristics of a male patient with a novel homozygous STAT5b mutationSolrun Vidarsdottir, Marie J E Walenkamp, Alberto M Pereira, et al.
Journal of the American Society of Nephrology : JASN|March 30, 2016
Inhibition of Activin Signaling Slows Progression of Polycystic Kidney DiseaseWouter N Leonhard, Steven J Kunnen, Anna J Plugge, et al.
European Journal of Human Genetics : EJHG|May 14, 2009
A new diagnostic workflow for patients with mental retardation and/or multiple congenital abnormalities: test arrays firstAntoinet C J Gijsbers, Janet Y K Lew, Cathy A J Bosch, et al.
Journal of the American Society of Nephrology : JASN|November 30, 1999
Aberrant splicing in the PKD2 gene as a cause of polycystic kidney diseaseD M Reynolds, T Hayashi, Y Cai, et al.
Cytogenetic and Genome Research|September 29, 2007
Variation of CNV distribution in five different ethnic populationsS J White, L E L M Vissers, A Geurts van Kessel, et al.
Leukemia|February 3, 1998
Detection of CBP rearrangements in acute myelogenous leukemia with t(8;16)R H Giles, J G Dauwerse, C Higgins, et al.
Pageof 40