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Clayton Smith

Showing results (41-50 of 352) with videos related to

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BMJ (Clinical Research Ed.)|February 3, 1990
Examination of fetuses after induced abortion for fetal abnormalityJ Clayton-Smith, P A Farndon, C McKeown, et al.
Clinical Dysmorphology|November 19, 2010
Cutaneous features in 17q21.31 deletion syndrome: a differential diagnosis for cardio-facio-cutaneous syndromeEmma Burkitt Wright, Dian Donnai, Diana Johnson, et al.
Journal of Medical Genetics|November 1, 1991
The non-deletion alpha thalassaemia/mental retardation syndrome: further support for X linkageD Donnai, J Clayton-Smith, R J Gibbons, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|September 27, 2015
In utero exposure to valproate increases the risk of isolated cleft palateAdam Jackson, Rebecca Bromley, James Morrow, et al.
Prenatal Diagnosis|May 1, 1994
Examination of fetuses after induced abortion for fetal abnormality--a follow-up studyA Medeira, A Norman, J Haslam, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|October 22, 2005
Dysmorphic features: an important clue to the diagnosis and severity of fetal anticonvulsant syndromesU Kini, N Adab, J Vinten, et al.
American Journal of Medical Genetics. Part A|March 4, 2017
Interrupted/bipartite clavicle as a diagnostic clue in Kabuki syndromeMaria Haanpää, Helena Schlecht, Gauri Batra, et al.
Neuropediatrics|April 12, 2003
Neuropsychological assessment of a group of UK patients with Cohen syndromeK E Chandler, M Moffett, J Clayton-Smith, et al.
Journal of Medical Genetics|August 14, 2014
Oculo-auriculo-vertebral spectrum: a review of the literature and genetic updateAna Beleza-Meireles, Jill Clayton-Smith, Jorge M Saraiva, et al.
European Journal of Medical Genetics|July 17, 2017
Confirmation that mutations in DDX59 cause an autosomal recessive form of oral-facial-digital syndrome: Further delineation of the DDX59 phenotype in two new familiesSara Faily, Rahat Perveen, Jill Urquhart, et al.
Pageof 36

Showing results (41-50 of 352) with videos related to

Sort By:
Pageof 36
BMJ (Clinical Research Ed.)|February 3, 1990
Examination of fetuses after induced abortion for fetal abnormalityJ Clayton-Smith, P A Farndon, C McKeown, et al.
Clinical Dysmorphology|November 19, 2010
Cutaneous features in 17q21.31 deletion syndrome: a differential diagnosis for cardio-facio-cutaneous syndromeEmma Burkitt Wright, Dian Donnai, Diana Johnson, et al.
Journal of Medical Genetics|November 1, 1991
The non-deletion alpha thalassaemia/mental retardation syndrome: further support for X linkageD Donnai, J Clayton-Smith, R J Gibbons, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|September 27, 2015
In utero exposure to valproate increases the risk of isolated cleft palateAdam Jackson, Rebecca Bromley, James Morrow, et al.
Prenatal Diagnosis|May 1, 1994
Examination of fetuses after induced abortion for fetal abnormality--a follow-up studyA Medeira, A Norman, J Haslam, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|October 22, 2005
Dysmorphic features: an important clue to the diagnosis and severity of fetal anticonvulsant syndromesU Kini, N Adab, J Vinten, et al.
American Journal of Medical Genetics. Part A|March 4, 2017
Interrupted/bipartite clavicle as a diagnostic clue in Kabuki syndromeMaria Haanpää, Helena Schlecht, Gauri Batra, et al.
Neuropediatrics|April 12, 2003
Neuropsychological assessment of a group of UK patients with Cohen syndromeK E Chandler, M Moffett, J Clayton-Smith, et al.
Journal of Medical Genetics|August 14, 2014
Oculo-auriculo-vertebral spectrum: a review of the literature and genetic updateAna Beleza-Meireles, Jill Clayton-Smith, Jorge M Saraiva, et al.
European Journal of Medical Genetics|July 17, 2017
Confirmation that mutations in DDX59 cause an autosomal recessive form of oral-facial-digital syndrome: Further delineation of the DDX59 phenotype in two new familiesSara Faily, Rahat Perveen, Jill Urquhart, et al.
Pageof 36