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Publications by J M Old
Prenatal Diagnosis of Ornithine Carbamoyl Transferase Deficiency Using a Gene Specific Probe.
Journal of Medical Genetics
Genetics
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Cloning of a Yeast Gene Coding for Arginine-Specific Carbamoyl-Phosphate Synthetase.
Proceedings of the National Academy of Sciences of the United States of America
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Imaging Farnesyl Protein Transferase Using a Topologically Activated Probe
Family Studies in Ornithine Transcarbamylase Deficiency.
Archives of Disease in Childhood
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Hyperammonaemia Due to Ornithine Transcarbamylase Deficiency
Archives of Disease in Childhood
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Atlas of Genetics and Cytogenetics in Oncology and Haematology
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Complete Ornithine Transcarbamylase Deficiency: A Cause of Lethal Neonatal Hyperammonemia
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Child Health
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Ornithine Transcarbamylase Deficiency: A Possible Risk Factor for Thrombosis
Blood
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First Trimester Prenatal Diagnosis of Smith-Lemli-Opitz Syndrome(7-Dehydrocholesterol Reductase Deficiency)
Pediatric Research
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Corrigendum: Specific Antibody Deficiency: Controversies in Diagnosis and Management
Frontiers in Immunology
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