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Philip Twiss

Showing results (1-10 of 13) with videos related to

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Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|March 21, 2019
Clinical Diagnosis of Classical Cornelia de Lange Syndrome Made From Postmortem Examination of Second Trimester Fetus With Novel <i>NIPBL</i> Pathogenic VariantJennifer Hague, Philip Twiss, Zoe Mead, et al.
Seminars in Fetal & Neonatal Medicine|November 12, 2013
Non-invasive prenatal testing for Down syndromePhilip Twiss, Melissa Hill, Rebecca Daley, et al.
International Journal of Cancer|July 2, 2009
The CDH1-160C>A polymorphism is a risk factor for colorectal cancerAlan M Pittman, Philip Twiss, Peter Broderick, et al.
Prenatal Diagnosis|February 25, 2015
Non-invasive prenatal diagnosis for cystic fibrosis: detection of paternal mutations, exploration of patient preferences and cost analysisMelissa Hill, Philip Twiss, Talitha I Verhoef, et al.
Journal of Medical Genetics|November 21, 2022
Conclusion of diagnostic odysseys due to inversions disrupting <i>GLI3</i> and <i>FBN1</i>Alistair T Pagnamenta, Jing Yu, Julie Evans, et al.
Human Mutation|October 16, 2010
Evaluation of germline BMP4 mutation as a cause of colorectal cancerSteven J Lubbe, Alan M Pittman, Cornelis Matijssen, et al.
Human Molecular Genetics|February 4, 2010
Fine-scale mapping of the 6p25.3 chronic lymphocytic leukaemia susceptibility locusDalemari Crowther-Swanepoel, Peter Broderick, Yussanne Ma, et al.
Genome Research|April 28, 2009
The colorectal cancer risk at 18q21 is caused by a novel variant altering SMAD7 expressionAlan M Pittman, Silvia Naranjo, Emily Webb, et al.
Plos Genetics|September 24, 2010
Allelic variation at the 8q23.3 colorectal cancer risk locus functions as a cis-acting regulator of EIF3HAlan M Pittman, Silvia Naranjo, Sanni E Jalava, et al.
Nature Communications|December 2, 2023
Selenoprotein deficiency disorder predisposes to aortic aneurysm formationErik Schoenmakers, Federica Marelli, Helle F Jørgensen, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|March 21, 2019
Clinical Diagnosis of Classical Cornelia de Lange Syndrome Made From Postmortem Examination of Second Trimester Fetus With Novel <i>NIPBL</i> Pathogenic VariantJennifer Hague, Philip Twiss, Zoe Mead, et al.
Seminars in Fetal & Neonatal Medicine|November 12, 2013
Non-invasive prenatal testing for Down syndromePhilip Twiss, Melissa Hill, Rebecca Daley, et al.
International Journal of Cancer|July 2, 2009
The CDH1-160C>A polymorphism is a risk factor for colorectal cancerAlan M Pittman, Philip Twiss, Peter Broderick, et al.
Prenatal Diagnosis|February 25, 2015
Non-invasive prenatal diagnosis for cystic fibrosis: detection of paternal mutations, exploration of patient preferences and cost analysisMelissa Hill, Philip Twiss, Talitha I Verhoef, et al.
Journal of Medical Genetics|November 21, 2022
Conclusion of diagnostic odysseys due to inversions disrupting <i>GLI3</i> and <i>FBN1</i>Alistair T Pagnamenta, Jing Yu, Julie Evans, et al.
Human Mutation|October 16, 2010
Evaluation of germline BMP4 mutation as a cause of colorectal cancerSteven J Lubbe, Alan M Pittman, Cornelis Matijssen, et al.
Human Molecular Genetics|February 4, 2010
Fine-scale mapping of the 6p25.3 chronic lymphocytic leukaemia susceptibility locusDalemari Crowther-Swanepoel, Peter Broderick, Yussanne Ma, et al.
Genome Research|April 28, 2009
The colorectal cancer risk at 18q21 is caused by a novel variant altering SMAD7 expressionAlan M Pittman, Silvia Naranjo, Emily Webb, et al.
Plos Genetics|September 24, 2010
Allelic variation at the 8q23.3 colorectal cancer risk locus functions as a cis-acting regulator of EIF3HAlan M Pittman, Silvia Naranjo, Sanni E Jalava, et al.
Nature Communications|December 2, 2023
Selenoprotein deficiency disorder predisposes to aortic aneurysm formationErik Schoenmakers, Federica Marelli, Helle F Jørgensen, et al.
Pageof 2