Werdnig-Hoffmann's infantile progressive muscular atrophy; clinical aspects, pathology, heredity and relation to Oppenheim's amyotonia congenita and other morbid conditions with laxity of joints or muscles in infants.

Werdnig-Hoffmann's infantile progressive muscular atrophy; clinical aspects, pathology, heredity and relation to Oppenheim's amyotonia congenita and other morbid conditions with laxity of joints or muscles in infants.

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Bibliographic Details
Author / Creator:	Brandt, Sven., author
Imprint:	Copenhagen, Munksgaard, 1950.
Description:	xiv, 328 pages illustrations.
Language:	English
Series:	Opera ex Domo Biologiae Hereditariae Humanae Universitatis Hafniensis, v. 22 Københavns universitet. Institut for human arvebiologi og eugenik. Opera 22.
Subject:	Muscular atrophy Infants -- Diseases Neuromuscular Diseases Infants -- Diseases. Muscular atrophy.
Format:	Print Book
URL for this record:	http://pi.lib.uchicago.edu/1001/cat/bib/3985054

Hidden Bibliographic Details
Notes:	"Translated from Danish by Hans Andersen, M.D." Includes bibliography. Resumé in English and Danish.

Mansueto

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Holdings details from Mansueto
Call Number:	QH431.A1C76 v.22
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