Rezultati - Jill Clayton‐Smith
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Angelman syndrome: a review of the clinical and genetic aspects od Jill Clayton‐Smith
Izdano 2003Revisão -
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Fetal valproate syndrome. od Jill Clayton‐Smith, Dian Donnai
Izdano 1995Artigo -
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Evolving phenotype of Marfan's syndrome od K. Lipscomb, Jill Clayton‐Smith, R Harris
Izdano 1997Artigo -
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Further Clinical Delineation of the MEF2C Haploinsufficiency Syndrome: Report on New Cases and Literature Review of Severe Neurodevelopmental Disorders Presenting with Seizures, Ab... od Irena Vrečar, Josie Innes, Elizabeth A. Jones, Helen Kingston, William Reardon, Bronwyn Kerr, Jill Clayton‐Smith, Sofia Douzgou
Izdano 2017Revisão -
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Diagnosing the cause of bilateral paediatric cataracts: comparison of standard testing with a next-generation sequencing approach od Mahmoud Musleh, Georgina Hall, I. Christopher Lloyd, Rachel Gillespie, S. Waller, Sofia Douzgou, Jill Clayton‐Smith, Elias Kehdi, Graeme Black, Jane Ashworth
Izdano 2016Artigo -
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A novel method for detecting uniparental disomy from trio genotypes identifies a significant excess in children with developmental disorders od Daniel A. King, Tomas Fitzgerald, Ray Miller, Natalie Canham, Jill Clayton‐Smith, Diana Johnson, Sahar Mansour, Fiona Stewart, Pradeep Vasudevan, Matthew E. Hurles
Izdano 2013Artigo -
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The prevalence of neurodevelopmental disorders in children prenatally exposed to antiepileptic drugs od 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
Izdano 2013Artigo -
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Iskalna orodja:
Sorodne teme
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