Prenatal Diagnosis of Hereditary Biochemical Disorders of Metabolism-Reference-Cited by-同舟云学术

Prenatal Diagnosis of Hereditary Biochemical Disorders of Metabolism

Published:1979 Issue: Volume: Page:209-367
ISSN:
Container-title:Genetic Disorders and the Fetus
language:
Short-container-title:

Author:

Milunsky Aubrey

Publisher

Springer US

Link

http://link.springer.com/content/pdf/10.1007/978-1-4684-3438-5_7.pdf

Reference1527 articles.

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2. Abe, K., Matsuda, I., Arashima, S., et al., 1976, Ultrastructural studies in fetal I-cell disease, Pediatr. Res. 10:669

3. Aberg, A., Mitelman, F., and Cantz, M., 1978, Cardiac puncture of fetus with Hurler’s disease avoiding abortion of unaffected co-twin, Lancet 2:990.

4. Abramov, A., Schorr, S., and Wolman, M., 1956, Generalized xanthomatosis with calcified adrenals. Am. J. Dis. Child. 91:282.

5. Advisory Committee to the Renal Transplant Registry, 1975, Renal transplantation in congenital and metabolic diseases: A report from the ASC/NIH Renal Transplant Registry, JAMA 232:148.

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