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W Reardon

Showing results (131-140 of 166) with videos related to

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Human Reproduction (Oxford, England)|December 20, 2005
Assisted reproductive therapies and imprinting disorders--a preliminary British surveyA G Sutcliffe, C J Peters, S Bowdin, et al.
Genomics|December 1, 1992
Localization of two genes for Usher syndrome type I to chromosome 11R J Smith, E C Lee, W J Kimberling, et al.
American Journal of Human Genetics|June 1, 1993
Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophyH G Harley, S A Rundle, J C MacMillan, et al.
European Journal of Pediatrics|December 14, 1999
Sacral dysgenesis associated with terminal deletion of chromosome 7q: a report of two familiesJ Wang, L Spitz, R Hayward, et al.
Genomics|December 1, 1992
Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11W J Kimberling, C G Möller, S Davenport, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Spectrum of craniosynostosis phenotypes associated with novel mutations at the fibroblast growth factor receptor 2 locusL J Pulleyn, W Reardon, D Wilkes, et al.
American Journal of Human Genetics|July 1, 1992
Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3)I Bach, H G Brunner, P Beighton, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|February 17, 2005
Outbreak of listeriosis among Mexican immigrants as a result of consumption of illicitly produced Mexican-style cheesePia D M MacDonald, Robert E Whitwam, Jackie D Boggs, et al.
Journal of Medical Genetics|January 3, 2001
Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing lossM J Houseman, L A Ellis, A Pagnamenta, et al.
Journal of Medical Genetics|August 1, 1997
Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosisW Reardon, D Wilkes, P Rutland, et al.
Pageof 17

Showing results (131-140 of 166) with videos related to

Sort By:
Pageof 17
Human Reproduction (Oxford, England)|December 20, 2005
Assisted reproductive therapies and imprinting disorders--a preliminary British surveyA G Sutcliffe, C J Peters, S Bowdin, et al.
Genomics|December 1, 1992
Localization of two genes for Usher syndrome type I to chromosome 11R J Smith, E C Lee, W J Kimberling, et al.
American Journal of Human Genetics|June 1, 1993
Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophyH G Harley, S A Rundle, J C MacMillan, et al.
European Journal of Pediatrics|December 14, 1999
Sacral dysgenesis associated with terminal deletion of chromosome 7q: a report of two familiesJ Wang, L Spitz, R Hayward, et al.
Genomics|December 1, 1992
Linkage of Usher syndrome type I gene (USH1B) to the long arm of chromosome 11W J Kimberling, C G Möller, S Davenport, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Spectrum of craniosynostosis phenotypes associated with novel mutations at the fibroblast growth factor receptor 2 locusL J Pulleyn, W Reardon, D Wilkes, et al.
American Journal of Human Genetics|July 1, 1992
Microdeletions in patients with gusher-associated, X-linked mixed deafness (DFN3)I Bach, H G Brunner, P Beighton, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|February 17, 2005
Outbreak of listeriosis among Mexican immigrants as a result of consumption of illicitly produced Mexican-style cheesePia D M MacDonald, Robert E Whitwam, Jackie D Boggs, et al.
Journal of Medical Genetics|January 3, 2001
Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing lossM J Houseman, L A Ellis, A Pagnamenta, et al.
Journal of Medical Genetics|August 1, 1997
Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosisW Reardon, D Wilkes, P Rutland, et al.
Pageof 17