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Archives of Neurology|November 1, 1984
Arthrogryposis multiplex congenita occurring with maternal multiple sclerosisI R Livingstone, G H SackMolecular Biology & Medicine|April 1, 1988
Serum amyloid A (SAA) gene variations in familial Mediterranean feverG H SackClinical Genetics|December 1, 1978
A dominantly inherited form of arthrogryposis multiplex congenita with unusual dermatoglyphicsG H SackJournal of Neurogenetics|April 1, 1984
Machado-Joseph disease in an American-Italian familyI R Livingstone, J SequeirosJournal De Genetique Humaine|December 1, 1983
Hereditary spastic paraplegia: a clinical and genetic study of cases in the north-east of EnglandI R Livingstone, D F RobertsAmerican Journal of Medical Genetics|August 1, 1985
Linear skin atrophy, scarring alopecia, anonychia, and tongue lesion: a "new" syndrome?J Sequeiros, G H SackBiochemical and Biophysical Research Communications|March 26, 1992
The human serum amyloid A locus SAA4 is a pseudogeneG H Sack, C C TalbotScandinavian Journal of Immunology|April 1, 1991
Highly polymorphic domains of the human serum amyloid A (SAA) gene GSAA1G H Sack, C C TalbotProteins|April 9, 1998
A fusion protein between serum amyloid A and staphylococcal nuclease--synthesis, purification, and structural studiesA K Meeker, G H SackPageof 5