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BMC Medical Genomics|May 10, 2018
A child with multiple congenital anomalies due to partial trisomy 7q22.1 → qter resulting from a maternally inherited balanced translocation: a case report and review of literatureC S Paththinige, N D Sirisena, U G I U Kariyawasam, et al.Lancet (London, England)|April 12, 1997
Prevalence of Pro250Arg mutation of fibroblast growth factor receptor 3 in coronal craniosynostosisD M Moloney, S A Wall, G J Ashworth, et al.The Journal of Rheumatology|May 1, 1995
Mild expression of fibrodysplasia ossificans progressiva: a report of 3 casesH B Janoff, J A Tabas, E M Shore, et al.Advances in Pediatrics|January 25, 2000
Syndromes associated with immunodeficiencyJ E Ming, E R Stiehm, J M GrahamAmerican Journal of Medical Genetics|December 30, 1996
Immunodeficiency as a component of recognizable syndromesJ E Ming, E R Stiehm, J M GrahamAmerican Journal of Human Genetics|February 1, 1991
In situ hybridization to cytogenetic bands of yeast artificial chromosomes covering 50% of human Xq24-Xq28 DNAV Montanaro, A Casamassimi, M D'Urso, et al.European Journal of Biochemistry|May 12, 2000
ARP3beta, the gene encoding a new human actin-related protein, is alternatively spliced and predominantly expressed in brain neuronal cellsP Jay, J L Bergé-Lefranc, A Massacrier, et al.Nature Genetics|October 15, 1998
Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-pairedS A Brown, D Warburton, L Y Brown, et al.Human Genetics|August 1, 1997
Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephalyE Roessler, D E Ward, K Gaudenz, et al.Clinical and Experimental Immunology|July 1, 1992
IL-6 enhances the generation of cytolytic T lymphocytes in the allogeneic mixed leucocyte reactionJ E Ming, R M Steinman, A Granelli-PipernoPageof 12