The Inheritance of Muscular Dystrophy: Further Observations
Overview
Authors
Affiliations
Richterich R, ROSIN S, Aebi U, Rossi E Am J Hum Genet. 1963; 15(2):133-54.
PMID: 17948483 PMC: 1932227.
SERUM ENZYME VARIATIONS AND HISTOLOGICAL ABNORMALITIES IN THE CARRIER STATE IN DUCHENNE DYSTROPHY.
Stephens J, Lewin E J Neurol Neurosurg Psychiatry. 1965; 28:104-8.
PMID: 14285647 PMC: 495868. DOI: 10.1136/jnnp.28.2.104.
Discrimination of genetic entities in muscular dystrophy.
Chung C, Morton N Am J Hum Genet. 1959; 11:339-59.
PMID: 13810212 PMC: 1932040.
Bibliography of human genetics.
Post R Am J Hum Genet. 1957; 9(4):331-49.
PMID: 13498002 PMC: 1932022.
X-linked Duchenne muscular dystrophy in an unusual family with manifesting carriers.
Kaladhar Reddy B, Anandavalli T, Reddi O Hum Genet. 1984; 67(4):460-2.
PMID: 6490012 DOI: 10.1007/BF00291412.