Carrier detection of urea cycle disorders. [electronic resource]
Producer: 19811122Description: 448-52 p. digitalISSN:- 0031-4005
- Amino Acid Metabolism, Inborn Errors -- genetics
- Ammonia -- blood
- Argininosuccinate Synthase -- blood
- Citrulline -- blood
- Female
- Genetic Carrier Screening
- Humans
- Infant, Newborn
- Male
- Ornithine Carbamoyltransferase Deficiency Disease
- Orotic Acid -- urine
- Pedigree
- Pregnancy
- Prenatal Diagnosis
- Urea -- metabolism
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
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