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S Malcolm

Showing results (121-130 of 271) with videos related to

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International Journal of Clinical Practice|May 20, 2014
Comparative safety and tolerability of duloxetine vs. pregabalin vs. duloxetine plus gabapentin in patients with diabetic peripheral neuropathic painG Irving, R J Tanenberg, J Raskin, et al.
Human Molecular Genetics|August 1, 1997
The TWIST gene, although not disrupted in Saethre-Chotzen patients with apparently balanced translocations of 7p21, is mutated in familial and sporadic casesC S Rose, P Patel, W Reardon, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|May 5, 1999
Toxicological consequences of feeding PCB congeners to infant rhesus (Macaca mulatta) and cynomolgus (Macaca fascicularis) monkeysD L Arnold, F Bryce, J Mes, et al.
Annals of Neurology|May 1, 1992
Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1)P J Hallam, A E Harding, J Berciano, et al.
Journal of Medical Genetics|June 1, 1992
Confirmation of an association between RFLPs at the transforming growth factor-alpha locus and non-syndromic cleft lip and palateS E Holder, G M Vintiner, B Farren, et al.
Proceedings. Biological Sciences|September 22, 1995
Human minisatellite loci composed of interspersed GGA-GGT triplet repeatsJ A Armour, M Crosier, S Malcolm, et al.
Human Molecular Genetics|July 1, 1997
The oral-facial-digital syndrome type 1 (OFD1), a cause of polycystic kidney disease and associated malformations, maps to Xp22.2-Xp22.3S A Feather, A S Woolf, D Donnai, et al.
Lancet (London, England)|April 2, 1988
Use of X chromosome inactivation analysis to establish carrier status for X-linked severe combined immunodeficiencyJ Goodship, S Malcolm, Y L Lau, et al.
Blood|June 15, 1991
Carrier detection in Wiskott-Aldrich syndrome: combined use of M27 beta for X-inactivation studies and as a linked probeJ Goodship, J Carter, T Espanol, et al.
American Journal of Human Genetics|January 1, 1990
Linkage of hereditary motor and sensory neuropathy type I to the pericentromeric region of chromosome 17H R Middleton-Price, A E Harding, C Monteiro, et al.
Pageof 28

Showing results (121-130 of 271) with videos related to

Sort By:
Pageof 28
International Journal of Clinical Practice|May 20, 2014
Comparative safety and tolerability of duloxetine vs. pregabalin vs. duloxetine plus gabapentin in patients with diabetic peripheral neuropathic painG Irving, R J Tanenberg, J Raskin, et al.
Human Molecular Genetics|August 1, 1997
The TWIST gene, although not disrupted in Saethre-Chotzen patients with apparently balanced translocations of 7p21, is mutated in familial and sporadic casesC S Rose, P Patel, W Reardon, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|May 5, 1999
Toxicological consequences of feeding PCB congeners to infant rhesus (Macaca mulatta) and cynomolgus (Macaca fascicularis) monkeysD L Arnold, F Bryce, J Mes, et al.
Annals of Neurology|May 1, 1992
Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1)P J Hallam, A E Harding, J Berciano, et al.
Journal of Medical Genetics|June 1, 1992
Confirmation of an association between RFLPs at the transforming growth factor-alpha locus and non-syndromic cleft lip and palateS E Holder, G M Vintiner, B Farren, et al.
Proceedings. Biological Sciences|September 22, 1995
Human minisatellite loci composed of interspersed GGA-GGT triplet repeatsJ A Armour, M Crosier, S Malcolm, et al.
Human Molecular Genetics|July 1, 1997
The oral-facial-digital syndrome type 1 (OFD1), a cause of polycystic kidney disease and associated malformations, maps to Xp22.2-Xp22.3S A Feather, A S Woolf, D Donnai, et al.
Lancet (London, England)|April 2, 1988
Use of X chromosome inactivation analysis to establish carrier status for X-linked severe combined immunodeficiencyJ Goodship, S Malcolm, Y L Lau, et al.
Blood|June 15, 1991
Carrier detection in Wiskott-Aldrich syndrome: combined use of M27 beta for X-inactivation studies and as a linked probeJ Goodship, J Carter, T Espanol, et al.
American Journal of Human Genetics|January 1, 1990
Linkage of hereditary motor and sensory neuropathy type I to the pericentromeric region of chromosome 17H R Middleton-Price, A E Harding, C Monteiro, et al.
Pageof 28