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Annemarie H van der Hout

Showing results (1-10 of 29) with videos related to

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Fertility and Sterility|November 25, 2011
IVF and retinoblastoma revisitedCharlotte J Dommering, Annemarie H van der Hout, Hanne Meijers-Heijboer, et al.
Human Mutation|August 31, 2002
Occurrence of deletion of a COL2A1 allele as the mutation in Stickler syndrome shows that a collagen type II dosage effect underlies this syndromeAnnemarie H Van Der Hout, Edwin Verlind, Frits A Beemer, et al.
Journal of Medical Genetics|April 2, 2014
RB1 mutation spectrum in a comprehensive nationwide cohort of retinoblastoma patientsCharlotte J Dommering, Berber M Mol, Annette C Moll, et al.
Neurogenetics|September 17, 2020
De novo ARHGEF9 missense variants associated with neurodevelopmental disorder in females: expanding the genotypic and phenotypic spectrum of ARHGEF9 disease in femalesMarcello Scala, Evelien Zonneveld-Huijssoon, Marianna Brienza, et al.
Familial Cancer|December 30, 2011
RB1 mutations and second primary malignancies after hereditary retinoblastomaCharlotte J Dommering, Tamara Marees, Annemarie H van der Hout, et al.
European Journal of Human Genetics : EJHG|January 31, 2008
Mutation screening of the Ectodysplasin-A receptor gene EDAR in hypohidrotic ectodermal dysplasiaAnnemarie H van der Hout, Grétel G Oudesluijs, Andrea Venema, et al.
Genes, Chromosomes & Cancer|November 20, 2013
High resolution SNP array profiling identifies variability in retinoblastoma genome stabilityBerber M Mol, Maarten P G Massink, Annemarie H van der Hout, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|June 10, 2016
Bias Explains Most of the Parent-of-Origin Effect on Breast Cancer Risk in BRCA1/2 Mutation CarriersJanet R Vos, Jan C Oosterwijk, Cora M Aalfs, et al.
Scientific Reports|April 30, 2016
Somatic genomic alterations in retinoblastoma beyond RB1 are rare and limited to copy number changesIrsan E Kooi, Berber M Mol, Maarten P G Massink, et al.
Human Mutation|December 26, 2003
DGGE-based whole-gene mutation scanning of the dystrophin gene in Duchenne and Becker muscular dystrophy patientsRobert M W Hofstra, Inge M Mulder, Rolf Vossen, et al.
Pageof 3

Showing results (1-10 of 29) with videos related to

Sort By:
Pageof 3
Fertility and Sterility|November 25, 2011
IVF and retinoblastoma revisitedCharlotte J Dommering, Annemarie H van der Hout, Hanne Meijers-Heijboer, et al.
Human Mutation|August 31, 2002
Occurrence of deletion of a COL2A1 allele as the mutation in Stickler syndrome shows that a collagen type II dosage effect underlies this syndromeAnnemarie H Van Der Hout, Edwin Verlind, Frits A Beemer, et al.
Journal of Medical Genetics|April 2, 2014
RB1 mutation spectrum in a comprehensive nationwide cohort of retinoblastoma patientsCharlotte J Dommering, Berber M Mol, Annette C Moll, et al.
Neurogenetics|September 17, 2020
De novo ARHGEF9 missense variants associated with neurodevelopmental disorder in females: expanding the genotypic and phenotypic spectrum of ARHGEF9 disease in femalesMarcello Scala, Evelien Zonneveld-Huijssoon, Marianna Brienza, et al.
Familial Cancer|December 30, 2011
RB1 mutations and second primary malignancies after hereditary retinoblastomaCharlotte J Dommering, Tamara Marees, Annemarie H van der Hout, et al.
European Journal of Human Genetics : EJHG|January 31, 2008
Mutation screening of the Ectodysplasin-A receptor gene EDAR in hypohidrotic ectodermal dysplasiaAnnemarie H van der Hout, Grétel G Oudesluijs, Andrea Venema, et al.
Genes, Chromosomes & Cancer|November 20, 2013
High resolution SNP array profiling identifies variability in retinoblastoma genome stabilityBerber M Mol, Maarten P G Massink, Annemarie H van der Hout, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|June 10, 2016
Bias Explains Most of the Parent-of-Origin Effect on Breast Cancer Risk in BRCA1/2 Mutation CarriersJanet R Vos, Jan C Oosterwijk, Cora M Aalfs, et al.
Scientific Reports|April 30, 2016
Somatic genomic alterations in retinoblastoma beyond RB1 are rare and limited to copy number changesIrsan E Kooi, Berber M Mol, Maarten P G Massink, et al.
Human Mutation|December 26, 2003
DGGE-based whole-gene mutation scanning of the dystrophin gene in Duchenne and Becker muscular dystrophy patientsRobert M W Hofstra, Inge M Mulder, Rolf Vossen, et al.
Pageof 3