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Publications by C H Rodeck

Prenatal Diagnosis of Ornithine Carbamoyl Transferase Deficiency Using a Gene Specific Probe.

Journal of Medical Genetics

English

Related publications

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

Multidisciplinary

English

Imaging Farnesyl Protein Transferase Using a Topologically Activated Probe

English

Family Studies in Ornithine Transcarbamylase Deficiency.

Archives of Disease in Childhood

English

Hyperammonaemia Due to Ornithine Transcarbamylase Deficiency

Archives of Disease in Childhood

English

Prenatal Diagnosis

Atlas of Genetics and Cytogenetics in Oncology and Haematology

Cancer Research

English

Complete Ornithine Transcarbamylase Deficiency: A Cause of Lethal Neonatal Hyperammonemia

Pediatric Research

English

Ornithine Transcarbamylase Deficiency: A Possible Risk Factor for Thrombosis

English

First Trimester Prenatal Diagnosis of Smith-Lemli-Opitz Syndrome(7-Dehydrocholesterol Reductase Deficiency)

Pediatric Research

English

Corrigendum: Specific Antibody Deficiency: Controversies in Diagnosis and Management

Frontiers in Immunology

English