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Journal of Medical Genetics|June 28, 2005
Breakpoints around the HOXD cluster result in various limb malformationsB Dlugaszewska, A Silahtaroglu, C Menzel, et al.American Journal of Human Genetics|December 1, 1991
Molecular definition of the shortest region of deletion overlap in the Langer-Giedion syndromeH J Lüdecke, C Johnson, M J Wagner, et al.Gene Expression Patterns : GEP|July 11, 2006
Detection of novel skeletogenesis target genes by comprehensive analysis of a Runx2(-/-) mouse modelJ Hecht, V Seitz, M Urban, et al.American Journal of Human Genetics|October 16, 1999
Mutation analysis of core binding factor A1 in patients with cleidocranial dysplasiaI Quack, B Vonderstrass, M Stock, et al.American Journal of Human Genetics|October 1, 1992
SSCP and segregation analysis of the human type X collagen gene (COL10A1) in heritable forms of chondrodysplasiaW A Sweetman, B Rash, B Sykes, et al.Pediatric Radiology|February 24, 2001
Multiple epiphyseal dysplasia: radiographic abnormalities correlated with genotypeS L Unger, M D Briggs, P Holden, et al.Genes, Chromosomes & Cancer|June 1, 1993
Characterization of two 11q23.3-11q24 deletions and mapping of associated anonymous DNA markersJ P Sanford, S N Sait, L Pan, et al.American Journal of Human Genetics|August 2, 2007
A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGINK Lehmann, P Seemann, F Silan, et al.Nature Genetics|December 30, 1999
Mutations in a new gene, encoding a zinc-finger protein, cause tricho-rhino-phalangeal syndrome type IP Momeni, G Glöckner, O Schmidt, et al.American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|September 12, 2013
TCR repertoire analysis by next generation sequencing allows complex differential diagnosis of T cell-related pathologyM Dziubianau, J Hecht, L Kuchenbecker, et al.Pageof 18