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Showing results (61-70 of 67) with videos related to

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American Journal of Human Genetics|January 1, 1987
Hepatic methionine adenosyltransferase deficiency in a 31-year-old manW A Gahl, J D Finkelstein, K D Mullen, et al.
American Journal of Human Genetics|March 21, 2000
Methionine adenosyltransferase I/III deficiency: novel mutations and clinical variationsM E Chamberlin, T Ubagai, S H Mudd, et al.
American Journal of Human Genetics|January 1, 1985
The natural history of homocystinuria due to cystathionine beta-synthase deficiencyS H Mudd, F Skovby, H L Levy, et al.
Journal of Inherited Metabolic Disease|June 1, 2006
S-adenosylhomocysteine hydrolase deficiency in a 26-year-old manN R M Buist, B Glenn, O Vugrek, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Persistent hypermethioninaemia with dominant inheritanceH J Blom, A J Davidson, J D Finkelstein, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
S-Adenosylhomocysteine hydrolase deficiency: a second patient, the younger brother of the index patient, and outcomes during therapyI Barić, M Cuk, K Fumić, et al.
Journal of Inherited Metabolic Disease|October 13, 2001
Glycine N-methyltransferase deficiency: a novel inborn error causing persistent isolated hypermethioninaemiaS H Mudd, R Cerone, M C Schiaffino, et al.
Pageof 7

Showing results (61-70 of 67) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 67 results.
American Journal of Human Genetics|January 1, 1987
Hepatic methionine adenosyltransferase deficiency in a 31-year-old manW A Gahl, J D Finkelstein, K D Mullen, et al.
American Journal of Human Genetics|March 21, 2000
Methionine adenosyltransferase I/III deficiency: novel mutations and clinical variationsM E Chamberlin, T Ubagai, S H Mudd, et al.
American Journal of Human Genetics|January 1, 1985
The natural history of homocystinuria due to cystathionine beta-synthase deficiencyS H Mudd, F Skovby, H L Levy, et al.
Journal of Inherited Metabolic Disease|June 1, 2006
S-adenosylhomocysteine hydrolase deficiency in a 26-year-old manN R M Buist, B Glenn, O Vugrek, et al.
Journal of Inherited Metabolic Disease|January 1, 1992
Persistent hypermethioninaemia with dominant inheritanceH J Blom, A J Davidson, J D Finkelstein, et al.
Journal of Inherited Metabolic Disease|January 26, 2006
S-Adenosylhomocysteine hydrolase deficiency: a second patient, the younger brother of the index patient, and outcomes during therapyI Barić, M Cuk, K Fumić, et al.
Journal of Inherited Metabolic Disease|October 13, 2001
Glycine N-methyltransferase deficiency: a novel inborn error causing persistent isolated hypermethioninaemiaS H Mudd, R Cerone, M C Schiaffino, et al.
Pageof 7