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Human Molecular Genetics|June 1, 1994
Localization of the gene encoding the alpha 2/delta-subunits of the L-type voltage-dependent calcium channel to chromosome 7q and analysis of the segregation of flanking markers in malignant hyperthermia susceptible familiesD E Iles, F Lehmann-Horn, S W Scherer, et al.Human Molecular Genetics|July 1, 1997
Translocation breakpoint maps 5 kb 3' from TWIST in a patient affected with Saethre-Chotzen syndromeI Krebs, I Weis, M Hudler, et al.Journal of Medical Genetics|September 10, 2003
Genetic mapping of a new Lafora progressive myoclonus epilepsy locus (EPM2B) on 6p22E M Chan, D E Bulman, A D Paterson, et al.G3 (Bethesda, Md.)|June 8, 2022
Chromosomal-level reference genome assembly of the North American wolverine (Gulo gulo luscus): a resource for conservation genomicsSi Lok, Timothy N H Lau, Brett Trost, et al.Autism Research : Official Journal of the International Society for Autism Research|January 22, 2011
A genotype resource for postmortem brain samples from the Autism Tissue ProgramRichard F Wintle, Anath C Lionel, Pingzhao Hu, et al.Journal of Neurodevelopmental Disorders|April 13, 2011
Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autismVeronica J Vieland, Joachim Hallmayer, Yungui Huang, et al.Blood|December 3, 1998
Molecular cytogenetic characterization of a critical region in bands 7q35-q36 commonly deleted in malignant myeloid disordersK Döhner, J Brown, U Hehmann, et al.American Journal of Medical Genetics. Part A|October 31, 2009
Screening of DNA methylation at the H19 promoter or the distal region of its ICR1 ensures efficient detection of chromosome 11p15 epimutations in Russell-Silver syndromeShin-Ichi Horike, Jose Carlos P Ferreira, Makiko Meguro-Horike, et al.Journal of the American Academy of Child and Adolescent Psychiatry|June 24, 2014
Biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variantsJoanna Martin, Miriam Cooper, Marian L Hamshere, et al.American Journal of Medical Genetics. Part A|September 13, 2017
HLX is a candidate gene for a pattern of anomalies associated with congenital diaphragmatic hernia, short bowel, and aspleniaSandra A Farrell, Sandi Sodhi, Christian R Marshall, et al.Pageof 88