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M Till

Showing results (131-140 of 152) with videos related to

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Annals of Thoracic Surgery Short Reports|January 10, 2025
Institutional Experience With Robotic Lobectomy After Neoadjuvant Immunotherapy and ChemotherapyShale J Mack, Hamza Rshaidat, Annie Ho, et al.
Nature Communications|March 17, 2022
Dynamics of plasmid-mediated niche invasion, immunity to invasion, and pheromone-inducible conjugation in the murine gastrointestinal tractHelmut Hirt, Kerryl E Greenwood-Quaintance, Aaron M T Barnes, et al.
Human Molecular Genetics|August 6, 2015
Conserved hippocampal cellular pathophysiology but distinct behavioural deficits in a new rat model of FXSSally M Till, Antonis Asiminas, Adam D Jackson, et al.
American Journal of Medical Genetics|November 15, 2000
Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: a second FG locus [FGS2]?S Briault, L Villard, U Rogner, et al.
Human Reproduction (Oxford, England)|July 8, 2011
Pregnancy outcomes in 188 French cases of prenatally diagnosed Klinefelter syndromeN Gruchy, F Vialard, M Decamp, et al.
Neurobiology of Disease|October 8, 2020
Sexually dimorphic patterns in electroencephalography power spectrum and autism-related behaviors in a rat model of fragile X syndromeHayes Wong, Alexander W M Hooper, Yosuke Niibori, et al.
Science Translational Medicine|May 31, 2019
Sustained correction of associative learning deficits after brief, early treatment in a rat model of Fragile X SyndromeAntonis Asiminas, Adam D Jackson, Susana R Louros, et al.
Clinical Genetics|May 20, 2014
Incidental findings on array comparative genomic hybridization: detection of carrier females of dystrophinopathy without any family historyK Nguyen, A Putoux, T Busa, et al.
American Journal of Human Genetics|October 12, 2001
Large-scale deletions and SMADIP1 truncating mutations in syndromic Hirschsprung disease with involvement of midline structuresJ Amiel, Y Espinosa-Parrilla, J Steffann, et al.
American Journal of Medical Genetics|January 31, 1998
A gene for FG syndrome maps in the Xq12-q21.31 regionS Briault, R Hill, A Shrimpton, et al.
Pageof 16

Showing results (131-140 of 152) with videos related to

Sort By:
Pageof 16
Annals of Thoracic Surgery Short Reports|January 10, 2025
Institutional Experience With Robotic Lobectomy After Neoadjuvant Immunotherapy and ChemotherapyShale J Mack, Hamza Rshaidat, Annie Ho, et al.
Nature Communications|March 17, 2022
Dynamics of plasmid-mediated niche invasion, immunity to invasion, and pheromone-inducible conjugation in the murine gastrointestinal tractHelmut Hirt, Kerryl E Greenwood-Quaintance, Aaron M T Barnes, et al.
Human Molecular Genetics|August 6, 2015
Conserved hippocampal cellular pathophysiology but distinct behavioural deficits in a new rat model of FXSSally M Till, Antonis Asiminas, Adam D Jackson, et al.
American Journal of Medical Genetics|November 15, 2000
Mapping of X chromosome inversion breakpoints [inv(X)(q11q28)] associated with FG syndrome: a second FG locus [FGS2]?S Briault, L Villard, U Rogner, et al.
Human Reproduction (Oxford, England)|July 8, 2011
Pregnancy outcomes in 188 French cases of prenatally diagnosed Klinefelter syndromeN Gruchy, F Vialard, M Decamp, et al.
Neurobiology of Disease|October 8, 2020
Sexually dimorphic patterns in electroencephalography power spectrum and autism-related behaviors in a rat model of fragile X syndromeHayes Wong, Alexander W M Hooper, Yosuke Niibori, et al.
Science Translational Medicine|May 31, 2019
Sustained correction of associative learning deficits after brief, early treatment in a rat model of Fragile X SyndromeAntonis Asiminas, Adam D Jackson, Susana R Louros, et al.
Clinical Genetics|May 20, 2014
Incidental findings on array comparative genomic hybridization: detection of carrier females of dystrophinopathy without any family historyK Nguyen, A Putoux, T Busa, et al.
American Journal of Human Genetics|October 12, 2001
Large-scale deletions and SMADIP1 truncating mutations in syndromic Hirschsprung disease with involvement of midline structuresJ Amiel, Y Espinosa-Parrilla, J Steffann, et al.
American Journal of Medical Genetics|January 31, 1998
A gene for FG syndrome maps in the Xq12-q21.31 regionS Briault, R Hill, A Shrimpton, et al.
Pageof 16