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American Journal of Medical Genetics. Part A
|
May 20, 2015
Prenatal diagnosis of fragile X syndrome complicated by full mutation retraction
Zornitza Stark, David Francis, Lydia Gaffney, et al.
NPJ Genomic Medicine
|
July 14, 2018
Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases
Michelle M Clark, Zornitza Stark, Lauge Farnaes, et al.
European Journal of Human Genetics : EJHG
|
June 21, 2024
Key informant perspectives on implementing genomic newborn screening: a qualitative study guided by the Action, Actor, Context, Target, Time framework
Erin Tutty, Alison D Archibald, Lilian Downie, et al.
Genes
|
April 10, 2019
Clinical and Molecular Differences between 4-Year-Old Monozygous Male Twins Mosaic for Normal, Premutation and Fragile X Full Mutation Alleles
Alison Pandelache, Emma K Baker, Solange M Aliaga, et al.
European Journal of Human Genetics : EJHG
|
February 7, 2020
Clinical genomic testing: what matters to key stakeholders?
Stephanie Best, Zornitza Stark, Peta Phillips, et al.
Prenatal Diagnosis
|
October 10, 2014
Apert syndrome: temporal lobe abnormalities on fetal brain imaging
Zornitza Stark, George McGillivray, Amanda Sampson, et al.
American Journal of Medical Genetics. Part A
|
November 29, 2015
Severe connective tissue laxity including aortic dilatation in Sotos syndrome
Rebecca L Hood, George McGillivray, Matthew F Hunter, et al.
American Journal of Medical Genetics. Part A
|
November 14, 2017
Expanding the phenotypic spectrum of TP63-related disorders including the first set of monozygotic twins
Tara Wenger, Dong Li, Margaret H Harr, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 27, 2017
Prospective comparison of the cost-effectiveness of clinical whole-exome sequencing with that of usual care overwhelmingly supports early use and reimbursement
Zornitza Stark, Deborah Schofield, Khurshid Alam, et al.
Archives of Disease in Childhood
|
October 23, 2024
Design and evaluation of a visual genomic explainer: a mixed-methods study
Grainne Butler, Camilla Andersen, Jim Buttery, et al.
Page
of 27
Search research articles
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Showing results (81-90 of 270) with videos related to
Sort By:
Page
of 27
American Journal of Medical Genetics. Part A
|
May 20, 2015
Prenatal diagnosis of fragile X syndrome complicated by full mutation retraction
Zornitza Stark, David Francis, Lydia Gaffney, et al.
NPJ Genomic Medicine
|
July 14, 2018
Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases
Michelle M Clark, Zornitza Stark, Lauge Farnaes, et al.
European Journal of Human Genetics : EJHG
|
June 21, 2024
Key informant perspectives on implementing genomic newborn screening: a qualitative study guided by the Action, Actor, Context, Target, Time framework
Erin Tutty, Alison D Archibald, Lilian Downie, et al.
Genes
|
April 10, 2019
Clinical and Molecular Differences between 4-Year-Old Monozygous Male Twins Mosaic for Normal, Premutation and Fragile X Full Mutation Alleles
Alison Pandelache, Emma K Baker, Solange M Aliaga, et al.
European Journal of Human Genetics : EJHG
|
February 7, 2020
Clinical genomic testing: what matters to key stakeholders?
Stephanie Best, Zornitza Stark, Peta Phillips, et al.
Prenatal Diagnosis
|
October 10, 2014
Apert syndrome: temporal lobe abnormalities on fetal brain imaging
Zornitza Stark, George McGillivray, Amanda Sampson, et al.
American Journal of Medical Genetics. Part A
|
November 29, 2015
Severe connective tissue laxity including aortic dilatation in Sotos syndrome
Rebecca L Hood, George McGillivray, Matthew F Hunter, et al.
American Journal of Medical Genetics. Part A
|
November 14, 2017
Expanding the phenotypic spectrum of TP63-related disorders including the first set of monozygotic twins
Tara Wenger, Dong Li, Margaret H Harr, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 27, 2017
Prospective comparison of the cost-effectiveness of clinical whole-exome sequencing with that of usual care overwhelmingly supports early use and reimbursement
Zornitza Stark, Deborah Schofield, Khurshid Alam, et al.
Archives of Disease in Childhood
|
October 23, 2024
Design and evaluation of a visual genomic explainer: a mixed-methods study
Grainne Butler, Camilla Andersen, Jim Buttery, et al.
Page
of 27