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News
NHS laboratory aims to pilot next-generation genetic sequencing...
www.progress.org.uk
... Dr Morag Shanks, Dr Alex Kwasniewska, Dr Jenny Taylor, Dr Anneke Seller, Dr Emily Packham, Dr Treena Cranston and Dr Penny Clouston.
Network Profiles
Interests
International study allows better prediction of risk of hereditary...
www.sciencedaily.com
... Terrilea Burnett, Therese Teitsch, Tsun Leung Chan, Tom Smyrk, Treena Cranston, Vasiliki Psofaki, Verena Steinke-Lange, Victor-Manuel Barbera.
Business Profiles
Researchgate: Treena Cranston
Leeds, London, United Kingdom
Books & Literature
Treena+Cranston | XanEdu Customization Platform
www.academicpub.com
clinical diagnosis of familial hypercholesterolaemia: relationship with plasma
lipid ...
Essential Readings In Health Psychology - Ogden, Jane - Google Books
books.google.de
... a previously aware population A randomized controlled trial Theresa Marteau,1 * Victoria Senior,1 Steve E. Humphries,8 Martin Bobrow,1o Treena Cranston,9 ...
Related Documents
A calcium-sensing receptor (CaSR) variant, Glu250Lys, present in...
www.endocrine-abstracts.org
Fadil Hannan 1, M Andrew Nesbit 1, Treena Cranston 2 & Rajesh Thakker 1. Author affiliations Mutational analysis of the calcium-sensing receptor (CaSR) is ...
GNA11 loss-of-function mutations cause familial hypocalciuric...
www.endocrine-abstracts.org
Fadil Hannan 1, M A Nesbit 1, Sarah Howles 1, Valerie Babinsky 1, Treena Cranston 2, Nigel Rust 1, Maurine Hobbs 3, Hunter Heath III 4 & Rajesh Thakker 1. Author
A PATIENT WITH AN APPARENTLY SPORADIC PHEOCHROMOCYTOMA WITH A...
www.proquest.com
Isabel Huguet, MD1; Treena Cranston, BSc2; Lisa Walker, MD3;. Niki Karavitaki, MSc, PhD, FRCP2; Ashley B. Grossman, BA, BSc, MD, FRCP, FMedSci2.
Uniparental isodisomy as a cause of the autoimmune polyendocrinopathy...
www.endocrine-abstracts.org
Uniparental isodisomy as a cause of the autoimmune polyendocrinopathy candidiasis ectodermal dystrophy (APECED) syndrome Treena Cranston 1, …
Scientific Publications
Use of multivariate analysis to suggest a new molecular...
www.ncbi.nlm.nih.gov
... , 1, 2 Dahmane Oukrif, 3 Daniel Rosmarin, 1, 4 Michal Presz, 4 Haitao Wang, 4 Hannah Pulker, 1, 5 Helen Lockstone, 6 Tarjei Hveem, 7, 8 Treena Cranston, 5 Havard
Publications
ARMC5 mutations are common in familial bilateral macronodular adrenal...
core.ac.uk
By Lucia Gagliardi, Andreas W. Schreiber, Christopher N. Hahn, Jinghua Feng, Treena Cranston, Hannah Boon, Cheri Hotu, Bergithe E. Oftedal, Richard ...
Mutational analysis in UK patients with a clinical diagnosis of...
link.springer.com
Treena Cranston (2) Marcus Allen (2) Helen Middleton-Price (2) Maryam C. Fernandez (3) Victoria Senior (4) Emma Hawe (1) Andrew Iversen (5) Richard Wray (6) Martin A
Use of multivariate analysis to suggest a new BioMedSearch
www.biomedsearch.com
Hannah Pulker,1,5 Helen Lockstone,6 Tarjei Hveem,7,8 Treena Cranston,5 Havard Danielsen,7,8 Marco Novelli,3. Brian Davidson,2 ...
Reports & Statements
Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3...
www.nature.com
Rajesh Thakker and colleagues show that missense mutations affecting codon 15 of AP2S1 cause familial hypocalciuric hypercalcemia type 3, a disorder of calcium...
Miscellaneous
Developing a diagnostic service for Stargardt disease – a feasibility...
slideplayer.com
Stargardt disease Autosomal recessive juvenile macular degeneration Prevalence of 1 in 10,000
Treena Cranston
endo.confex.com
Churchill Hospital Oxford Molecular Genetics Laboratory Papers: A Loss-of-Function G-Protein Alpha-11-Thr54Met Mutation Causes Familial Hypocalciuric Hypercalcemia ...
Familial Hypocalciuric Hypercalcemia(FHH) CASR Disorders - ppt video...
slideplayer.com
Objectives: Introduction to FHH and CaSR disorders Presentaion Genetics Diagnosis
Activity - PanelApp
panelapp.extge.co.uk
... Foulger (Genomics England curator) marked GDNF as ready. 29 Aug 2017, Familial ovarian cancer · RAD51D, Treena Cranston (Oxford) reviewed RAD51D.
(PDF) Detection Rate of Pathogenic Mutations in ABCA4 Using Direct...
www.academia.edu
Detection Rate of Pathogenic Mutations in ABCA4 Using Direct Sequencing: Clinical and Research Implications
Do Patients with Bilateral Adrenal Nodules Represent …
endo.confex.com
Do Patients with Bilateral Adrenal Nodules Represent an Early Form of ARMC5-Mediated Bilateral Macronodular Hyperplasia? ... Holly Emms 2, Treena Cranston 3 and ...
Confusing genes: a patient with MEN2A and Cushing's disease
www.growkudos.com
Auditi Naziat, Niki Karavitaki, Rajesh Thakker, Olaf Ansorge, Greg Sadler, Fergus Gleeson, Treena Cranston, Ann McCormack, Ashley B Grossman, Brian Shine.
OR Confex
endo.confex.com
Sarah A Howles, BMBCh 1, M Andrew Nesbit, PhD 2, Fadil M Hannan, PhD 3, Angela Rogers 1, Sian E Piret 1, Treena Cranston 4, Mushtaqur Rahman 5 and Rajesh V Thakker 1
Adaptor protein-2 sigma subunit mutations causing familial...
pure.qub.ac.uk
author = "Hannan, {Fadil M.} and Howles, {Sarah A.} and Angela Rogers and Treena Cranston and Gorvin, {Caroline M.} and Babinsky, {Valerie N.} and Reed, ...
Altmetric – Mutations in AP2S1 cause familial hypocalciuric...
www.altmetric.com
M Andrew Nesbit, Fadil M Hannan, Sarah A Howles, Anita A C Reed, Treena Cranston, Clare E Thakker, Lorna Gregory, Andrew J Rimmer, Nigel Rust, Una ...
Confusing genes: a patient with MEN2A and Cushing's disease | Read by...
read.qxmd.com
Auditi Naziat, Niki Karavitaki, Rajesh Thakker, Olaf Ansorge, Greg Sadler, Fergus Gleeson, Treena Cranston, Ann McCormack, Ashley B Grossman, Brian Shine.
Most recent papers in the shared collection...
read.qxmd.com
Fadil M Hannan, Sarah A Howles, Angela Rogers, Treena Cranston, Caroline M Gorvin, Valerie N Babinsky, Anita A Reed, Clare E Thakker, ...
Exemplare: Mutations in AP2S1 cause familial hypocalciuric...
ebusca.uv.mx
Main Authors: M Andrew Nesbit, Fadil M Hannan, Sarah A Howles, Anita A C Reed, Treena Cranston, Clare E Thakker, Lorna Gregory, Andrew J Rimmer, Nigel ...
Molecular and clinical analysis of a neonatal severe...
eje.bioscientifica.com
The authors would like to thank Prof. Raj Thakker and Dr Treena Cranston (University of Oxford) for their assistance with the gene sequencing, ...
November 1, Issue of JAMA Ophthalmology | JAMA Network
jamanetwork.com
Read the November 1, issue. Volume 130, Number 11
PPT - Developing a diagnostic service for Stargardt disease – a...
www.slideserve.com
Developing a diagnostic service for Stargardt disease – a feasibility study. Emily Packham Oxford Regional Molecular Genetics Laboratory. Introduction ....
Mutational analysis in UK patients with a clinical diagnosis of...
www.infona.pl
Steve E. Humphries, Treena Cranston, Marcus Allen, Helen Middleton-Price, Maryam C. Fernandez, Victoria Senior, Emma Hawe, Andrew Iversen, Richard ...
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