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Genomics|September 1, 1992
Assignment of genes encoding a unique cytokine (IL12) composed of two unrelated subunits to chromosomes 3 and 5D Sieburth, E W Jabs, J A Warrington, et al.Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|February 5, 2000
Second-trimester molecular prenatal diagnosis of sporadic Apert syndrome following suspicious ultrasound findingsJ C Ferreira, S M Carter, P S Bernstein, et al.Biological Psychiatry|April 21, 2001
Regional cortical white matter reductions in velocardiofacial syndrome: a volumetric MRI analysisW R Kates, C P Burnette, E W Jabs, et al.Cell|November 5, 1993
A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosisE W Jabs, U Müller, X Li, et al.American Journal of Medical Genetics|October 1, 1993
Saethre-Chotzen syndrome with familial translocation at chromosome 7p22C S Reid, L E McMorrow, D M McDonald-McGinn, et al.Cytogenetics and Cell Genetics|January 1, 1994
Localization of a putative human brain sodium channel gene (SCN1A) to chromosome band 2q24M S Malo, B J Blanchard, J M Andresen, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 4, 2000
Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndromeR A Norris, K K Scott, C S Moore, et al.The Journal of Biological Chemistry|May 6, 1994
Complete cDNA sequence of a human dioxin-inducible mRNA identifies a new gene subfamily of cytochrome P450 that maps to chromosome 2T R Sutter, Y M Tang, C L Hayes, et al.Nature Genetics|November 1, 1994
Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2E W Jabs, X Li, A F Scott, et al.Genomics|May 1, 1993
The CEPH consortium linkage map of human chromosome 13A M Bowcock, S C Gerken, R I Barnes, et al.Pageof 11