scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0022-3476(67)80205-1 |
P698 | PubMed publication ID | 4383264 |
P2093 | author name string | Passarge E | |
McAdams AJ | |||
P2860 | cites work | MUTANT MICE (QUAKING AND JIMPY) WITH DEFICIENT MYELINATION IN THE CENTRAL NERVOUS SYSTEM | Q28590426 |
Oral-facial-digital syndrome, with polycystic kidneys and liver: pathological and cytogenetic studies | Q33585403 | ||
STUDIES OF A FAMILY WITH THE ORAL-FACIAL-DIGITAL SYNDROME. | Q39662891 | ||
Metachromatic leukodystrophy (sulfatide lipidoses) cultured in vitro. | Q51214940 | ||
A syndrome of multiple developmental defects including polycystic kidneys and intrahepatic biliary dysgenesis in 2 siblings. | Q52348415 | ||
Retinal dysplasia | Q74846758 | ||
PELIZAEUS-MERZBACHER DISEASE. A STUDY IN NOSOLOGY | Q76786526 | ||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | liver cirrhosis | Q147778 |
P304 | page(s) | 691-702 | |
P577 | publication date | 1967-11-01 | |
P1433 | published in | The Journal of Pediatrics | Q7743611 |
P1476 | title | Cerebro-hepato-renal syndrome. A newly recognized hereditary disorder of multiple congenital defects, including sudanophilic leukodystrophy, cirrhosis of the liver, and polycystic kidneys. | |
P478 | volume | 71 |
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