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American Journal of Human Genetics|September 1, 1977
The Hunter syndrome in females: is there an autosomal recessive form of iduronate sulfatase deficiency?E F Neufeld, I Liebaers, C J Epstein, et al.Pediatric Research|August 1, 1976
Iduronate sulfatase activity in serum, lymphocytes, and fibroblasts--simplified diagnosis of the Hunter syndromeI Liebaers, E NeufeldJournal of Medical Genetics|December 1, 1977
Hunter syndrome presenting as macrocephaly and hydrocephalusS Yatziv, C J EpsteinClinical Genetics|May 1, 1977
Mild and severe Hunter syndrome (MPS II) within the same sibshipsS Yatziv, R P Erickson, C J EpsteinNature|January 26, 1978
X-chromosome inactivation during differentiation of female teratocarcinoma stem cells in vitroG R Martin, C J Epstein, B Travis, et al.Enzyme|January 1, 1984
Prenatal diagnosis of inborn errors of metabolism. Present status and new approachesE Vamos, I LiebaersBailliere'S Clinical Obstetrics and Gynaecology|August 6, 1998
The genetics of male infertility in relation to cystic fibrosisW Lissens, I LiebaersEuropean Journal of Pediatrics|January 18, 1979
Pre and post axial polysyndactyly, microcephaly and ptosisD Engelhard, S YatzivClinical Genetics|April 1, 1981
An unusual form of metachromatic leukodystrophy in three siblingsS Yatziv, A RussellScience (New York, N.Y.)|December 5, 1980
Correction of enzyme deficiency in mice by allogeneic bone marrow transplantation with total lymphoid irradiationS Slavin, S YatzivPageof 50