Clinical, biochemical, and ultrastructural studies in a case of chondrodystrophy presenting the I-cell phenotype in tissue culture-Reference-Cited by-同舟云学术

Clinical, biochemical, and ultrastructural studies in a case of chondrodystrophy presenting the I-cell phenotype in tissue culture

Published:1971-09 Issue:3 Volume:79 Page:366-378
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Tondeur M.,Vamos-Hurwitz E.,Mockel-Pohl S.,Dereume J.P.,Cremer N.,Loeb H.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference41 articles.

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3. Gargoylism (Hunter-Hurler disease, dysostosis multiplex, lipochondrodystrophy). Prenatal and neonatal bone lesions and their early postnatal evolution;Caffey;Amer. J. Roentgen.,1952

4. Hepatic ultrastructure in the Hurler syndrome;Callahan;Amer. J. Path.,1966

5. Hurler's syndrome. A genetic study in cell culture;Danes;J. Exp. Med.,1966

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