| scholarly article | Q13442814 |
| P356 | DOI | 10.1056/NEJM198502143120717 |
| P698 | PubMed publication ID | 3969102 |
| P2093 | author name string | Moser AB | |
| Moser HW | |||
| Jackson LG | |||
| Hajra AK | |||
| Larsen JW Jr | |||
| Datta NS | |||
| Powers J | |||
| P433 | issue | 7 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 445-446 | |
| P577 | publication date | 1985-02-01 | |
| P1433 | published in | The New England Journal of Medicine | Q582728 |
| P1476 | title | Prenatal diagnosis of Zellweger cerebrohepatorenal syndrome | |
| P478 | volume | 312 |
| Q38623776 | Adrenoleukodystrophy and other peroxisomal disorders that affect the nervous system, including new observations on L-pipecolic acid oxidase in primates |
| Q57386868 | Biochemical abnormalities in rhizomelic chondrodysplasia punctata |
| Q50571924 | Infantile Refsum disease: an inherited peroxisomal disorder. Comparison with Zellweger syndrome and neonatal adrenoleukodystrophy. |
| Q39730039 | Peroxisomal disorders: a newly recognised group of genetic diseases |
| Q38237404 | Prenatal and perinatal diagnosis of peroxisomal disorders |
| Q34622861 | Purification, properties, and immunocytochemical localization of human liver peroxisomal enoyl-CoA hydratase/3-hydroxyacyl-CoA dehydrogenase |
| Q55485687 | The eye and inherited metabolic disease: a review. |
| Q38599534 | The pathologist's perspective of genetic disease. Malformations and dysmorphology |
| Q36652090 | The peroxisome and the eye |
| Q39598541 | Zellweger syndrome: biochemical procedures in diagnosis, prevention and treatment |
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