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W Reardon

Showing results (81-90 of 166) with videos related to

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Journal of Medical Genetics|April 1, 1997
Fluorescent in situ hybridisation (FISH) for hemizygous deletion at the elastin locus in patients with isolated supravalvular aortic stenosisH Fryssira, R Palmer, K A Hallidie-Smith, et al.
Nature Genetics|September 1, 1994
Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndromeW Reardon, R M Winter, P Rutland, et al.
Journal of Medical Genetics|September 3, 2002
Mutation in KCNQ1 that has both recessive and dominant characteristicsA Murray, F Potet, C Bellocq, et al.
Clinical Dysmorphology|July 12, 2001
Three new European cases of urofacial (Ochoa) syndromeS Garcia-Minaur, F Oliver, J M Yanez, et al.
European Journal of Medical Genetics|March 15, 2006
Decreased cholesterol synthesis as a possible aetiological factor in malformations of trisomy 18Wayne W K Lam, J Kirk, N Manning, et al.
Human Molecular Genetics|July 1, 1997
Elastin: genomic structure and point mutations in patients with supravalvular aortic stenosisM Tassabehji, K Metcalfe, D Donnai, et al.
Personality and Mental Health|September 28, 2016
Measuring child personality when child personality was not measured: Application of a thin-slice approachJennifer L Tackett, Avanté J Smack, Kathrin Herzhoff, et al.
Clinical Dysmorphology|January 1, 1995
The natural history of human dermatosparaxis (Ehlers-Danlos syndrome type VIIC)W Reardon, R M Winter, L T Smith, et al.
American Journal of Medical Genetics|October 1, 1994
New autosomal dominant form of spondyloepiphyseal dysplasia presenting with atlanto-axial instabilityW Reardon, C M Hall, D G Shaw, et al.
Journal of Medical Genetics|March 1, 1995
Saethre-Chotzen syndrome associated with balanced translocations involving 7p21: three further familiesA O Wilkie, S P Yang, D Summers, et al.
Pageof 17

Showing results (81-90 of 166) with videos related to

Sort By:
Pageof 17
Journal of Medical Genetics|April 1, 1997
Fluorescent in situ hybridisation (FISH) for hemizygous deletion at the elastin locus in patients with isolated supravalvular aortic stenosisH Fryssira, R Palmer, K A Hallidie-Smith, et al.
Nature Genetics|September 1, 1994
Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndromeW Reardon, R M Winter, P Rutland, et al.
Journal of Medical Genetics|September 3, 2002
Mutation in KCNQ1 that has both recessive and dominant characteristicsA Murray, F Potet, C Bellocq, et al.
Clinical Dysmorphology|July 12, 2001
Three new European cases of urofacial (Ochoa) syndromeS Garcia-Minaur, F Oliver, J M Yanez, et al.
European Journal of Medical Genetics|March 15, 2006
Decreased cholesterol synthesis as a possible aetiological factor in malformations of trisomy 18Wayne W K Lam, J Kirk, N Manning, et al.
Human Molecular Genetics|July 1, 1997
Elastin: genomic structure and point mutations in patients with supravalvular aortic stenosisM Tassabehji, K Metcalfe, D Donnai, et al.
Personality and Mental Health|September 28, 2016
Measuring child personality when child personality was not measured: Application of a thin-slice approachJennifer L Tackett, Avanté J Smack, Kathrin Herzhoff, et al.
Clinical Dysmorphology|January 1, 1995
The natural history of human dermatosparaxis (Ehlers-Danlos syndrome type VIIC)W Reardon, R M Winter, L T Smith, et al.
American Journal of Medical Genetics|October 1, 1994
New autosomal dominant form of spondyloepiphyseal dysplasia presenting with atlanto-axial instabilityW Reardon, C M Hall, D G Shaw, et al.
Journal of Medical Genetics|March 1, 1995
Saethre-Chotzen syndrome associated with balanced translocations involving 7p21: three further familiesA O Wilkie, S P Yang, D Summers, et al.
Pageof 17