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News
Big day for brave Hayley | Daily Mail Online
www.dailymail.co.uk
Like most four-year-olds, Hayley Okines loves dancing to Kylie and watching cartoons. But because of an incurable ageing disease she is not expected to see her...
New cardiac genetic testing panels • healthcare-in-europe.com
healthcare-in-europe.com
As new cardiac genetic testing panels become available, cardiologists have been warned not to lose sight of the importance of comprehensive clinical...
Newsletter|XP Support Group
xpsupportgroup.org.uk
Dr Shehla Mohammed (Consultant Clinical Geneticist and Head of Genetics Service) · Dr Isabel Garrood (Clinical Neuropsychologist) · Dr Niseth Sheth ...
Network Profiles
LinkedIn: Shehla Mohammed | LinkedIn
View Shehla Mohammed's (United Kingdom) professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Shehla Mohammed ...
LinkedIn: Shehla Mohammed - Programme Associate - PHG …
Bekijk het profiel van Shehla Mohammed op LinkedIn, de grootste professionele community ter wereld. Shehla Mohammed heeft 12 banen functies op zijn of haar profiel.
Interests
In the genome, an answer to a mysterious movement disorder
www.sciencedaily.com
Children with a rather mysterious movement disorder can have hundreds of attacks every day in which they inexplicably make sudden movements or sudden changes...
Business Profiles
Researchgate: Shehla Mohammed
Leeds, London, United Kingdom
Shehla Mohammed director information. Free company director check.
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Shehla Mohammed - free Company Director Summary including all company appointments. Instant free Director Report for Risk Scores, County Court Judgements,...
Education
Shehla Mohammed - Research Portal, King's College, London
kclpure.kcl.ac.uk
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance
Shehla Mohammed - Research Outputs - Research Portal, King's...
kclpure.kcl.ac.uk
Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia. Deciphering Developmental Disorders Study, UK10K Consortium, NIHR ...
Projects
Shehla Mohammed is fundraising for Noah's Ark Children's ...www.justgiving.com › fundraising › shehla-mohammed1
www.justgiving.com
... ask if you would be willing to sponsor our team: “The Great Ascenders” (Paula Sullivan, Cristina Dias, Sarah Ross, Alison Lashwood and Shehla Mohammed).
Shehla Mohammed is fundraising for XP Support Group
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JustGiving - the easiest way to fundraise and donate to charity online
Books & Literature
Arterial tortuosity syndrome : 40 new families and literature review
biblio.ugent.be
... Stanislas Lyonnet, Helen Michael, Pamela Moceri, Shehla Mohammed, Laura Muiño Mosquera, Sheela Nampoothiri, Karin Pichler, Katrina ...
Rare Hereditary Cancers: Diagnosis and Management - Google Books
books.google.no
This book approaches the differential diagnosis and management of rare, hereditary cancer syndromes from a practical angle, addressing the issues pertinent to...
The Secret Life of Fat: The Science Behind the Body's Least...
books.google.no
A biochemist shows how we can finally control our fat—by understanding how it works. Fat is not just excess weight, but actually a dynamic, smart, and...
脂肪的祕密生命：最不為人知的器官脂肪背後的科學與它對身體的影響 - 席薇亞．塔拉(Sylvia Tara) - Google Books
books.google.no
... 甚至因肥胖引起的併發症提早離開人世。負責治療萊拉的醫療團隊中,有一位名為樹拉,穆罕默德( Shehla Mohammed )的臨床遺傳學家希望在她出院前再放手一搏 ...
Related Documents
CiteSeerX — RESEARCH Open Access
citeseerx.ist.psu.edu
BibTeX @MISC{Ahn_researchopen, author = {Joo Wook Ahn and Kathy Mann and Sally Walsh and Marwa Shehab and Sarah Hoang and Zoe Docherty and Shehla Mohammed …
Marfan’s syndrome and related aortopathies Shehla Mohammed -...
vdocuments.mx
Marfan’s syndrome and related aortopathies Shehla Mohammed Marfan’s syndrome Common multisystem connective tissue disorder 1 in Altered body proportions ...
CiteSeerX — with normal karyotype
citeseerx.ist.psu.edu
with normal karyotype ... Zabot and Arnaud Josiane and Lydie Burglen and Chris Bennett and Daniel Riconda and Richard Fisher and Ra Janssens and Shehla Mohammed ...
Shehla Mohammed - Academia.edu
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Academia.edu is a place to share and follow research.
Scientific Publications
A Distinct Genotype of XP Complementation Group A - PubMedpubmed.ncbi.nlm.nih.gov › ...
pubmed.ncbi.nlm.nih.gov
Mieran Sethi , Shaheen Haque , Heather Fawcett , Jonathan F Wing , Natalie Chandler , Shehla Mohammed , Ian M Frayling , Paul G Norris , David McGibbon ...
Clinical expression of Menkes disease in females with normal...
ojrd.biomedcentral.com
Shehla Mohammed. Department of Medical Genetics, University Medical Center Utrecht, PO Box , Utrecht, AB, 3508, The Netherlands.
Advances in Genetic Testing for Hereditary Cancer Syndromespubmed.ncbi.nlm.nih.gov › ...
pubmed.ncbi.nlm.nih.gov
2016;205: doi: _1. Authors. Ellen Thomas , Shehla Mohammed. Affiliations. 1 Department of Clinical Genetics, Guy's and St ...
Validation and implementation of array comparative genomic...
molecularcytogenetics.biomedcentral.com
Joo Wook Ahn,; Kathy Mann,; Sally Walsh,; Marwa Shehab,; Sarah Hoang,; Zoe Docherty,; Shehla Mohammed and; Caroline Mackie OgilvieEmail author.
Publications
Publications Authored by Mohammed Shehla | PubFacts
www.pubfacts.com
Publications Authored by Mohammed Shehla
p53 Protein Detected By Immunohistochemical Staining is Not Always...
www.hindawi.com
The expression of the tumour suppressor gene p53 was analyzed in a variety of human solid tumours by immunohistochemistry and direct DNA sequencing. Positive...
Advances in Genetic Testing for Hereditary Cancer Syndromes |...
link.springer.com
The ability to identify genetic mutations causing an increased risk of cancer represents the first widespread example of personalised medicine, in which...
Reports & Statements
Meet the 13 most powerful Muslim women in Britain | The Timeless LIGHT
thetimelesslight.wordpress.com
Dr Shehla Mohammed Consultant clinical geneticist. Dr Yasmin Naqushbandi Medical director, Barking, Havering and Redbridge NHS Trust.
Mutation of the RAD51C gene in a Fanconi anemia–like disorder |...
www.nature.com
Christopher Mathew and colleagues report a homozygous germline mutation of RAD51C in a Fanconi anemia-like disorder. Mutation of RAD51C, encoding a protein...
Miscellaneous
Shehla MOHAMMED | LinkedIn
www.linkedin.com
View Shehla MOHAMMED's professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Shehla MOHAMMED discover …
Marfan’s syndrome and related aortopathies Shehla Mohammed. - ppt...
slideplayer.com
Marfan's syndrome and related aortopathies Shehla Mohammed.
MS SHEHLA MOHAMMED director information. Free director information....
companycheck.co.uk
MS SHEHLA MOHAMMED - INACTIVE - Director ID is And address is - A free Director Summary including all company appointments.
Shehla Mohammed | Guy's and St Thomas' NHS Foundation Trust
www.guysandstthomas.nhs.uk
Shehla Mohammed is a consultant clinical geneticist and head of service
Dr Shehla MOHAMMED - Orphanetwww.orpha.net › cgi-bin › Directory_Professionals › M...
www.orpha.net
Dr Shehla MOHAMMED. Activities registered with Orphanet : Coordinator of expert centre - Clinical expert - Director of department; E-mail : email; Phone : ...
Pin by shehla mohammed on drawings | Pets cats, Beautiful cats, Petswww.pinterest.co.uk › pin
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May 30, This Pin was discovered by shehla mohammed. Discover (and save!) your own Pins on Pinterest.
Shehla Mohammed (ma ) – Profil | Pinterest
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See what Shehla Mohammed (ma ) has discovered on Pinterest, the world's biggest collection of ideas.
"The genomic landscape of balanced cytogenetic abnormalities...
digitalrepository.unm.edu
Shehla Mohammed ... Sjors Middelkamp; Liya R Mikami; Emily Moe; Shehla Mohammed; Tarja Mononen; Megan E Mortenson; Graciela Moya; ...
A systematic, large-scale resequencing screen of X-chromosome coding...
mdanderson.elsevierpure.com
... Jenny Moon ; Josef Parnau ; Shehla Mohammed ; John L. Tolmie ; Cheryl Shoubridge ; Mark Corbett ; Alison Gardner ; Eric Haan ; Sinitdhorn Rujirabanjerd ...
JCI - Welcome
www.jci.org
Hemanth Tummala, Amanda Walne, Laura Collopy, Shirleny Cardoso, Josu de la Fuente, Sarah Lawson, James Powell, Nicola Cooper, Alison Foster, Shehla Mohammed, …
JCI - Poly(A)-specific ribonuclease deficiency impacts telomere...
www.jci.org
· ... Josu de la Fuente, Sarah Lawson, James Powell, Nicola Cooper, Alison Foster, Shehla Mohammed, Vincent Plagnol, Thomas Vulliamy, Inderjeet Dokal ...
- Document - An isolated case of lissencephaly caused by the ...go.gale.com › i.do
go.gale.com
Authors: David S Millar [1]; Carolyn Tysoe [2]; Lazarus P Lazarou [3]; Daniela T Pilz [3]; Shehla Mohammed [4]; Katharine Anderson [5]; Nadia Chuzhanova [6]; ...
(PDF) Monozygotic twins discordant for frontonasal malformation |...
www.academia.edu
· Shehla Mohammed + 2. Shehla Mohammed. Marc Swan. Andrew Wilkie. connect to download. Get pdf. Monozygotic twins discordant for frontonasal …
Altmetric – Recessive mutations in EPG5 cause Vici syndrome, a...
www.altmetric.com
... Jozef Hertecant, Miguel Del Campo, Stefan Buk, Istvan Bodi, Hans-Hilmar Goebel, Caroline A Sewry, Stephen Abbs, Shehla Mohammed, Dragana Josifova , ...
An Evaluation of the Effectiveness of a Semi-automatic ...www.metasystems-probes.com › publications › may2008
www.metasystems-probes.com
Philippa C May, Caroline Mackie Ogilvie, Shehla Mohammed, Zoe Docherty, Richard Peter Hall. Karyotyping is currently the #gold##standard# test for the ...
Clinical expression of Menkes disease in females with normal...
pure.au.dk
... Daniel Riconda and Richard Fisher and Sandra Janssens and Shehla Mohammed and Margreet Ausems and Zeynep T{\"u}mer and Nina Horn and Jensen, ...
(PDF) Polymicrogyria and deletion 22q11.2 syndrome: Window to the...
www.academia.edu
Shehla Mohammed. Marie McDonald. Cathy Stevens. Neil Stoodley. ß Wiley-Liss, Inc. American Journal of Medical Genetics Part A 140A:2416 – (
Xeroderma pigmentosum (XP) team
www.guysandstthomas.nhs.uk
Dr Shehla Mohammed - consultant clinical geneticist; Dr Paola Giunti - consultant neurologist; Ms Susie Morley - consultant ophthalmologist and oculoplastic surgeon;
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