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Archives of Otolaryngology--Head & Neck Surgery|September 20, 2006
Antenatal carbimazole and choanal atresia: a new embryopathyDennis Wolf, Nicola Foulds, Hamid DayaAmerican Journal of Medical Genetics. Part A|April 17, 2008
Severe Marfan syndrome due to FBN1 exon deletionsMoira Blyth, Nicola Foulds, Claire Turner, et al.American Journal of Medical Genetics. Part A|December 4, 2004
Carbimazole embryopathy: an emerging phenotypeNicola Foulds, Ian Walpole, Frances Elmslie, et al.American Journal of Medical Genetics. Part A|May 20, 2011
Early pontocerebellar hypoplasia with vanishing testes: A new syndrome?Christopher Anderson, Justin H Davies, Lilias Lamont, et al.Neuromuscular Disorders : NMD|December 5, 2023
HNRNPA2B1 myopathy presenting in a family with an early onset oculopharyngeal muscular dystrophy-like phenotypeLiam S Carroll, Sarah Ennis, Nicola Foulds, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 5, 2013
Genetic medicine and incidental findings: it is more complicated than deciding whether to disclose or notGillian Crawford, Nicola Foulds, Angela Fenwick, et al.American Journal of Medical Genetics. Part A|November 18, 2008
A novel 2.43 Mb deletion of 7q11.22-q11.23Moira Blyth, Sarah Beal, Shuwen Huang, et al.Epilepsia|December 19, 2019
Diagnosis of pyridoxine-dependent epilepsy in an adult presenting with recurrent status epilepticusChinar Osman, Nicola Foulds, David Hunt, et al.American Journal of Medical Genetics. Part A|April 11, 2003
A female case of Sedaghatian type spondylometaphyseal dysplasiaNicola Foulds, Jo Fairhurst, I Karen Temple, et al.American Journal of Medical Genetics. Part A|September 4, 2015
Two further patients with the 1q24 deletion syndrome expand the phenotype: A possible role for the miR199-214 cluster in the skeletal features of the conditionTazeen Ashraf, Morag N Collinson, Joanna Fairhurst, et al.Pageof 6