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J Mulley

Showing results (21-30 of 28) with videos related to

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American Journal of Human Genetics|May 1, 1992
Fragile-X syndrome: unique genetics of the heritable unstable elementS Yu, J Mulley, D Loesch, et al.
Journal of Medical Genetics|December 1, 1991
Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile siteR I Richards, K Holman, H Kozman, et al.
Epilepsia|July 18, 2002
How mutations in the nAChRs can cause ADNFLE epilepsyD Bertrand, F Picard, S Le Hellard, et al.
Nature Genetics|May 13, 1999
A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardationK Merienne, S Jacquot, S Pannetier, et al.
American Journal of Medical Genetics|July 12, 1996
Seventh International Workshop on the Fragile X and X-linked Mental RetardationL Tranebjaerg, H A Lubs, M Borghgraef, et al.
American Journal of Medical Genetics|October 26, 2000
9th international workshop on fragile X syndrome and X-linked mental retardationJ P Fryns, M Borghgraef, T W Brown, et al.
Cell|April 13, 1999
Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromesM F McDermott, I Aksentijevich, J Galon, et al.
Biorxiv : the Preprint Server for Biology|July 15, 2024
The sensory shark: high-quality morphological, genomic and transcriptomic data for the small-spotted catshark <i>Scyliorhinus canicula</i> reveal the molecular bases of sensory organ evolution in jawed vertebratesH Mayeur, J Leyhr, J Mulley, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
American Journal of Human Genetics|May 1, 1992
Fragile-X syndrome: unique genetics of the heritable unstable elementS Yu, J Mulley, D Loesch, et al.
Journal of Medical Genetics|December 1, 1991
Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile siteR I Richards, K Holman, H Kozman, et al.
Epilepsia|July 18, 2002
How mutations in the nAChRs can cause ADNFLE epilepsyD Bertrand, F Picard, S Le Hellard, et al.
Nature Genetics|May 13, 1999
A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardationK Merienne, S Jacquot, S Pannetier, et al.
American Journal of Medical Genetics|July 12, 1996
Seventh International Workshop on the Fragile X and X-linked Mental RetardationL Tranebjaerg, H A Lubs, M Borghgraef, et al.
American Journal of Medical Genetics|October 26, 2000
9th international workshop on fragile X syndrome and X-linked mental retardationJ P Fryns, M Borghgraef, T W Brown, et al.
Cell|April 13, 1999
Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromesM F McDermott, I Aksentijevich, J Galon, et al.
Biorxiv : the Preprint Server for Biology|July 15, 2024
The sensory shark: high-quality morphological, genomic and transcriptomic data for the small-spotted catshark <i>Scyliorhinus canicula</i> reveal the molecular bases of sensory organ evolution in jawed vertebratesH Mayeur, J Leyhr, J Mulley, et al.
Pageof 3