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Clinician Barriers and Facilitators to Routine HIV Testing: A Systematic Review of the Literature

Journal of the International Association of Providers of AIDS Care, 2020-01, Vol.19, p.2325958220936014-2325958220936014

2020

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A genetic study of Wilson's disease in the United Kingdom

Brain (London, England : 1878), 2013-05, Vol.136 (Pt 5), p.1476-1487

2013

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Next Generation Sequencing in Newborn Screening in the United Kingdom National Health Service

International journal of neonatal screening, 2019-12, Vol.5 (4), p.40-40

2019

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Computer-based rhythm and timing training in severe, stroke-induced arm hemiparesis

The American journal of occupational therapy, 2011-01, Vol.65 (1), p.96-100

2011

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New pedigrees and novel mutation expand the phenotype of REEP1-associated hereditary spastic paraplegia (HSP)

Neurogenetics, 2009-04, Vol.10 (2), p.105-110

2009

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The In-Between: Unforgettable Encounters During Life's Final Moments

Journal of palliative medicine, 2024-02, Vol.27 (2), p.288

Dalton, Heather Ann

2024

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A deliberative study of public attitudes towards sharing genomic data within NHS genomic medicine services in England

Public understanding of science (Bristol, England), 2020-10, Vol.29 (7), p.702-717

2020

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TO033VERY EARLY-ONSET AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE DUE TO BI-ALLELIC MUTATIONS IN PKD1 AND PKD2

Nephrology, dialysis, transplantation, 2017-05, Vol.32 (suppl_3), p.iii94-iii94

2017

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Unexplained fractures in infancy: looking for fragile bones

Archives of Disease in Childhood, 2007-03, Vol.92 (3), p.251-256

2007

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Fetal mesenchymal stem-cell engraftment in bone after in utero transplantation in a patient with severe osteogenesis imperfecta

Transplantation, 2005-06, Vol.79 (11), p.1607-1614

2005

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Identifying functionally important aberrations of Neurofibromin-1 (NF1) in non-small cell lung cancer (NSCLC)

European journal of surgical oncology, 2018-03, Vol.44, p.S36-S36

2018

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Identifying functionally important aberrations of Neurofibromin-1 (NF1) in non-small cell lung cancer (NSCLC)

European journal of surgical oncology, 2017-11, Vol.43 (11), p.2233-2233

2017

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PPIB Mutations Cause Severe Osteogenesis Imperfecta

American journal of human genetics, 2009-10, Vol.85 (4), p.521-527

2009

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Mutation analysis of COL1A1 and COL1A2 in patients diagnosed with osteogenesis imperfecta type I-IV

Human mutation, 2006-07, Vol.27 (7), p.716-716

2006

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Attachment of human bone cells to tissue culture polystyrene and to unmodified polystyrene: the effect of surface chemistry upon initial cell attachment

Journal of biomaterials science. Polymer ed., 1994-01, Vol.5 (3), p.245-257

1994

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Genetic testing in the assessment of living related kidney donors at risk of autosomal dominant polycystic kidney disease

Transplantation, 2015-05, Vol.99 (5), p.1023-1029

2015

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The emerging fragile X premutation phenotype: Evidence from the domain of social cognition

Brain and cognition, 2005-02, Vol.57 (1), p.53-60

2005

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Age-dependent cognitive changes in carriers of the fragile X syndrome

Cortex, 2008-06, Vol.44 (6), p.628-636

2008

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Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations

American journal of medical genetics. Part A, 2016-12, Vol.170A (12), p.3150-3156

2016

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Social deprivation, population dependency ratio and an extended hospital episode — Insights from acute medicine

European journal of internal medicine, 2015-11, Vol.26 (9), p.714-719

2015

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Role of the heparin binding domain of fibronectin in attachment and spreading of human bone-derived cells

Journal of cell science, 1995-05, Vol.108 ( Pt 5) (5), p.2083-2092

1995

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Glycogen storage disease type IX: High variability in clinical phenotype

Molecular genetics and metabolism, 2007-09, Vol.92 (1), p.88-99

2007

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Mutational analysis of the GYS2 gene in patients diagnosed with ketotic hypoglycaemia

Journal of Pediatric Endocrinology and Metabolism, 2012-10, Vol.25 (9), p.963-967

2012

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CRTAP mutation in a patient with Cole-Carpenter syndrome

American journal of medical genetics. Part A, 2015-03, Vol.167A (3), p.587-591

2015

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Genotype-phenotype study in type V osteogenesis imperfecta

Clinical dysmorphology, 2013-07, Vol.22 (3), p.93-101

2013

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Clinician Barriers and Facilitators to Routine HIV Testing: A Systematic Review of the Literature

A genetic study of Wilson's disease in the United Kingdom

Next Generation Sequencing in Newborn Screening in the United Kingdom National Health Service

Computer-based rhythm and timing training in severe, stroke-induced arm hemiparesis

New pedigrees and novel mutation expand the phenotype of REEP1-associated hereditary spastic paraplegia (HSP)

The In-Between: Unforgettable Encounters During Life's Final Moments

A deliberative study of public attitudes towards sharing genomic data within NHS genomic medicine services in England

TO033VERY EARLY-ONSET AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE DUE TO BI-ALLELIC MUTATIONS IN PKD1 AND PKD2

Unexplained fractures in infancy: looking for fragile bones

Fetal mesenchymal stem-cell engraftment in bone after in utero transplantation in a patient with severe osteogenesis imperfecta

Identifying functionally important aberrations of Neurofibromin-1 (NF1) in non-small cell lung cancer (NSCLC)

Identifying functionally important aberrations of Neurofibromin-1 (NF1) in non-small cell lung cancer (NSCLC)

PPIB Mutations Cause Severe Osteogenesis Imperfecta

Mutation analysis of COL1A1 and COL1A2 in patients diagnosed with osteogenesis imperfecta type I-IV

Attachment of human bone cells to tissue culture polystyrene and to unmodified polystyrene: the effect of surface chemistry upon initial cell attachment

Genetic testing in the assessment of living related kidney donors at risk of autosomal dominant polycystic kidney disease

The emerging fragile X premutation phenotype: Evidence from the domain of social cognition

Age-dependent cognitive changes in carriers of the fragile X syndrome

Phenotypic variability in patients with osteogenesis imperfecta caused by BMP1 mutations

Social deprivation, population dependency ratio and an extended hospital episode — Insights from acute medicine

Role of the heparin binding domain of fibronectin in attachment and spreading of human bone-derived cells

Glycogen storage disease type IX: High variability in clinical phenotype

Mutational analysis of the GYS2 gene in patients diagnosed with ketotic hypoglycaemia

CRTAP mutation in a patient with Cole-Carpenter syndrome

Genotype-phenotype study in type V osteogenesis imperfecta

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