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Human Molecular Genetics|July 1, 1993
Genomic organization of the sequence coding for fibrillin, the defective gene product in Marfan syndromeL Pereira, M D'Alessio, F Ramirez, et al.
Journal of Medical Genetics|September 1, 1995
Mitochondrial DNA does not appear to influence the congenital onset type of myotonic dystrophyJ Poulton, H G Harley, J Dasmahapatra, et al.
Journal of Medical Genetics|March 1, 1991
Prenatal diagnosis of osteogenesis imperfecta by identification of the concordant collagen 1 alleleJ R Lynch, D Ogilvie, L Priestley, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 2001
Meis1a suppresses differentiation by G-CSF and promotes proliferation by SCF: potential mechanisms of cooperativity with Hoxa9 in myeloid leukemiaK R Calvo, P S Knoepfler, D B Sykes, et al.
The Journal of Antibiotics|July 1, 1984
Bacterial production of 7-formamidocephalosporins. Isolation and structure determinationP D Singh, M G Young, J H Johnson, et al.
Laboratory Medicine|March 2, 2023
Comprehensive Next-Generation Sequencing Testing in a Patient with TEMPI SyndromeFlavia Guimaraes Nunes Rosado, Danijela Lekovic, Jeffrey Gagan, et al.
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