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Stephanie K Allen

Showing results (1-10 of 7) with videos related to

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Best Practice & Research. Clinical Obstetrics & Gynaecology|September 10, 2024
Chapter 2: Non-invasive prenatal diagnosisStephanie K Allen, Samantha Doyle
Plos One|November 13, 2015
A Non-Invasive Droplet Digital PCR (ddPCR) Assay to Detect Paternal CFTR Mutations in the Cell-Free Fetal DNA (cffDNA) of Three Pregnancies at Risk of Cystic Fibrosis via Compound HeterozygosityEmmanuel Debrand, Alexandra Lykoudi, Elizabeth Bradshaw, et al.
Genetics Research|September 2, 2020
Cytogenomic results following high-chance non-invasive prenatal testing: a UK national auditFiona S Togneri, Stephanie K Allen, Kathy Mann, et al.
European Journal of Human Genetics : EJHG|May 20, 2020
EMQN best practice guidelines for genetic testing in dystrophinopathiesCarl Fratter, Raymond Dalgleish, Stephanie K Allen, et al.
Genetics Research|December 10, 2019
Implementation of cell-free DNA-based non-invasive prenatal testing in a National Health Service Regional Genetics LaboratoryFiona S Togneri, Mark D Kilby, Elizabeth Young, et al.
Prenatal Diagnosis|December 8, 2023
Diagnosis of inborn errors of metabolism through prenatal exome sequencing with targeted analysis for fetal structural anomaliesStephanie K Allen, Natalie J Chandler, Esther Kinning, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|August 31, 2011
Implementation and experience of an alternative QF-PCR and MLPA diagnostic strategy to detect chromosomal abnormalities in fetal and neonatal pathology samplesLouise S McClelland, Stephanie K Allen, Simon A Larkins, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Best Practice & Research. Clinical Obstetrics & Gynaecology|September 10, 2024
Chapter 2: Non-invasive prenatal diagnosisStephanie K Allen, Samantha Doyle
Plos One|November 13, 2015
A Non-Invasive Droplet Digital PCR (ddPCR) Assay to Detect Paternal CFTR Mutations in the Cell-Free Fetal DNA (cffDNA) of Three Pregnancies at Risk of Cystic Fibrosis via Compound HeterozygosityEmmanuel Debrand, Alexandra Lykoudi, Elizabeth Bradshaw, et al.
Genetics Research|September 2, 2020
Cytogenomic results following high-chance non-invasive prenatal testing: a UK national auditFiona S Togneri, Stephanie K Allen, Kathy Mann, et al.
European Journal of Human Genetics : EJHG|May 20, 2020
EMQN best practice guidelines for genetic testing in dystrophinopathiesCarl Fratter, Raymond Dalgleish, Stephanie K Allen, et al.
Genetics Research|December 10, 2019
Implementation of cell-free DNA-based non-invasive prenatal testing in a National Health Service Regional Genetics LaboratoryFiona S Togneri, Mark D Kilby, Elizabeth Young, et al.
Prenatal Diagnosis|December 8, 2023
Diagnosis of inborn errors of metabolism through prenatal exome sequencing with targeted analysis for fetal structural anomaliesStephanie K Allen, Natalie J Chandler, Esther Kinning, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|August 31, 2011
Implementation and experience of an alternative QF-PCR and MLPA diagnostic strategy to detect chromosomal abnormalities in fetal and neonatal pathology samplesLouise S McClelland, Stephanie K Allen, Simon A Larkins, et al.
Pageof 1