Результати пошуку - Jill Clayton‐Smith
- Показ 1 - 20 результатів із 109
- На наступну сторінку
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1
Angelman syndrome: a review of the clinical and genetic aspects за авторством Jill Clayton‐Smith
Опубліковано 2003Revisão -
2
Fetal valproate syndrome. за авторством Jill Clayton‐Smith, Dian Donnai
Опубліковано 1995Artigo -
3
Angelman syndrome. за авторством Jill Clayton‐Smith, Marcus Pembrey
Опубліковано 1992Artigo -
4
Evolving phenotype of Marfan's syndrome за авторством K. Lipscomb, Jill Clayton‐Smith, R Harris
Опубліковано 1997Artigo -
5
Practice guidelines for the molecular analysis of Prader-Willi and Angelman syndromes за авторством Simon Ramsden, Jill Clayton‐Smith, Rachael Birch, Karin Buiting
Опубліковано 2010Artigo -
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Oculo-auriculo-vertebral spectrum: a review of the literature and genetic update за авторством Ana Beleza‐Meireles, Jill Clayton‐Smith, Jorge Saraiva, May Tassabehji
Опубліковано 2014Revisão -
8
AUTISM SPECTRUM DISORDERS FOLLOWING IN UTERO EXPOSURE TO ANTIEPILEPTIC DRUGS за авторством Rebecca Bromley, G. E. Mawer, Jill Clayton‐Smith, Gus A. Baker
Опубліковано 2008Artigo -
9
Molecular mechanisms in Angelman syndrome: a survey of 93 patients. за авторством Christopher T. Chan, Jill Clayton‐Smith, Xingbo Cheng, Jess Buxton, T. Webb, Marcus Pembrey, S Malcolm
Опубліковано 1993Artigo -
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Coats' disease of the retina (unilateral retinal telangiectasis) caused by somatic mutation in the NDP gene: a role for norrin in retinal angiogenesis за авторством Graeme Black, Rahat Perveen, Richard Bonshek, Mark Cahill, Jill Clayton-Smith, I. Christopher Lloyd, David McLeod
Опубліковано 1999Artigo -
12
Further Clinical Delineation of the MEF2C Haploinsufficiency Syndrome: Report on New Cases and Literature Review of Severe Neurodevelopmental Disorders Presenting with Seizures, Ab... за авторством Irena Vrečar, Josie Innes, Elizabeth A. Jones, Helen Kingston, William Reardon, Bronwyn Kerr, Jill Clayton‐Smith, Sofia Douzgou
Опубліковано 2017Revisão -
13
Interchromosomal Insertional Translocation at Xq26.3 Alters<i>SOX3</i>Expression in an Individual With XX Male Sex Reversal за авторством Bryan P. Haines, James Hughes, Mark Corbett, Marie Shaw, Josie Innes, Leena Patel, Jozef Gécz, Jill Clayton‐Smith, Paul Q. Thomas
Опубліковано 2015Artigo -
14
Diagnosing the cause of bilateral paediatric cataracts: comparison of standard testing with a next-generation sequencing approach за авторством Mahmoud Musleh, Georgina Hall, I. Christopher Lloyd, Rachel Gillespie, S. Waller, Sofia Douzgou, Jill Clayton‐Smith, Elias Kehdi, Graeme Black, Jane Ashworth
Опубліковано 2016Artigo -
15
Prevalence of fetal alcohol spectrum disorder in Greater Manchester, UK: An active case ascertainment study за авторством Robyn McCarthy, Raja Mukherjee, Kate M. Fleming, Jonathan Green, Jill Clayton‐Smith, Alan D. Price, Clare S. Allely, Penny A. Cook
Опубліковано 2021Artigo -
16
Deletions in the<i>VPS13B</i>(<i>COH1</i>) gene as a cause of Cohen syndrome за авторством Irina Balikova, A‐E Lehesjoki, Thomy de Ravel, Bernard Thienpont, Kate Chandler, Jill Clayton‐Smith, A L Träskelin, J-P. Fryns, Joris Vermeesch
Опубліковано 2009Artigo -
17
A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders за авторством Daniel A. King, Tomas Fitzgerald, Ray Miller, Natalie Canham, Jill Clayton‐Smith, Diana Johnson, Sahar Mansour, Fiona Stewart, Pradeep Vasudevan, Matthew E. Hurles
Опубліковано 2013Artigo -
18
The prevalence of neurodevelopmental disorders in children prenatally exposed to antiepileptic drugs за авторством Rebecca Bromley, G. E. Mawer, Michelle Briggs, Christopher P. Cheyne, Jill Clayton‐Smith, Marta García‐Fiñana, Rachel Kneen, S. B. Lucas, Rebekah Shallcross, Gus A. Baker, Gus A. Baker, Michelle Briggs, Rebecca Bromley, Jill Clayton‐Smith, Pete Dixon, Alan Fryer, Alison Gummery, Rachel Kneen, Lydia Kerr, S. B. Lucas, G. E. Mawer, Rebekah Shallcross
Опубліковано 2013Artigo -
19
Assisted reproductive therapies and imprinting disorders—a preliminary British survey за авторством Alastair Sutcliffe, Catherine Peters, Sarah Bowdin, I. Karen Temple, William Reardon, Lisa M Wilson, Jill Clayton‐Smith, L A Brueton, Wendy Bannister, Eamonn R. Maher
Опубліковано 2005Artigo -
20
Monotherapy treatment of epilepsy in pregnancy: congenital malformation outcomes in the child за авторством Jennifer Weston, Rebecca Bromley, Cerian F Jackson, Naghme Adab, Jill Clayton‐Smith, J Greenhalgh, Juliet Hounsome, Andrew McKay, Catrin Tudur Smith, Anthony G Marson
Опубліковано 2016Revisão
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Пов'язані теми
Biology
Genetics
Gene
Medicine
Phenotype
Pediatrics
Mutation
Internal medicine
Psychiatry
Epilepsy
Pregnancy
Pathology
Carbamazepine
Exome sequencing
Lamotrigine
Psychology
Missense mutation
Chromosome
Haploinsufficiency
Exome
Genotype
Intellectual disability
Autism
Bioinformatics
Computational biology
Fetus
Loss function
Observational study
Genetic testing
Phenytoin