Dubowitz V
Postgrad Med J. 2011; 41(476):332-46.
PMID: 21313711
PMC: 2483018.
DOI: 10.1136/pgmj.41.476.332.
Richterich R, ROSIN S, Aebi U, Rossi E
Am J Hum Genet. 1963; 15(2):133-54.
PMID: 17948483
PMC: 1932227.
Prior T, Bridgeman S
J Mol Diagn. 2005; 7(3):317-26.
PMID: 16049303
PMC: 1867542.
DOI: 10.1016/S1525-1578(10)60560-0.
ROTTHAUWE H, Kowalewski S
Klin Wochenschr. 1965; 43:158-63.
PMID: 14258512
DOI: 10.1007/BF01484508.
Wilson K, Evans K, Carter C
Br Med J. 1965; 1(5437):750-3.
PMID: 14248444
PMC: 2166169.
DOI: 10.1136/bmj.1.5437.750.
SEVERE MUSCULAR DYSTROPHY IN GIRLS.
Smith A, MCILWAINE C
Br Med J. 1965; 1(5436):674.
PMID: 14245201
PMC: 2166379.
DOI: 10.1136/bmj.1.5436.674.
SEVERE MUSCULAR DYSTROPHY IN GIRLS.
Johnston H
J Med Genet. 1964; 1(2):79-81.
PMID: 14234109
PMC: 1012751.
SERUM ENZYME STUDIES IN MUSCLE DISEASE. III. SERUM CREATINE KINASE ACTIVITY IN RELATIVES OF PATIENTS WITH THE DUCHENNE TYPE OF MUSCULAR DYSTROPHY.
Pearce J, PENNINGTON R, Walton J
J Neurol Neurosurg Psychiatry. 1964; 27:181-5.
PMID: 14175282
PMC: 495722.
DOI: 10.1136/jnnp.27.3.181.
Sources of error in the biochemical diagnosis of muscular dystrophy.
Thomson W
J Neurol Neurosurg Psychiatry. 1962; 25:191-202.
PMID: 14037852
PMC: 495443.
DOI: 10.1136/jnnp.25.3.191.
Aldolase activity in the plasma or serum of normal children and families with muscular dystrophy.
Clayton B, Wilson K, Carter C
Arch Dis Child. 1963; 38:208-14.
PMID: 14021638
PMC: 2019036.
DOI: 10.1136/adc.38.199.208.
Serum enzyme activity in muscular dystrophy.
Thomson W, LEYBURN P, Walton J
Br Med J. 1960; 2(5208):1276-81.
PMID: 13776665
PMC: 2097052.
DOI: 10.1136/bmj.2.5208.1276.
A genetic study of Duchenne muscular dystrophy in West Midlands.
Bundey S
J Med Genet. 1981; 18(1):1-7.
PMID: 7252996
PMC: 1048649.
DOI: 10.1136/jmg.18.1.1.
Incidence of Duchenne muscular dystrophy in New South Wales and Australian Capital Territory.
Cowan J, Macdessi J, Stark A, MORGAN G
J Med Genet. 1980; 17(4):245-9.
PMID: 7205898
PMC: 1048563.
DOI: 10.1136/jmg.17.4.245.
Epidemiology of Duchenne muscular dystrophy in the province of Turin.
Bertolotto A, De Marchi M, Doriguzzi C, Mongini T, Monnier C, Palmucci L
Ital J Neurol Sci. 1981; 2(1):81-4.
PMID: 6977513
DOI: 10.1007/BF02351692.
The genetic status of mothers of isolated cases of Duchenne muscular dystrophy.
Lane R, ROBINOW M, Roses A
J Med Genet. 1983; 20(1):1-11.
PMID: 6842530
PMC: 1048978.
DOI: 10.1136/jmg.20.1.1.
Duchenne muscular dystrophy: pathogenetic aspects and genetic prevention.
Moser H
Hum Genet. 1984; 66(1):17-40.
PMID: 6365739
DOI: 10.1007/BF00275183.
Detection of carriers of benign X-linked muscular dystrophy.
EMERY A, Clack E, Simon S, Taylor J
Br Med J. 1967; 4(5578):522-3.
PMID: 6065987
PMC: 1749119.
DOI: 10.1136/bmj.4.5578.522.
[A benign recessiv X-chromosomal hereditary muscular dystrophy. II. Examinations of female carriers].
ROTTHAUWE H, Kowalewski S
Humangenetik. 1966; 3(1):30-40.
PMID: 5986053
DOI: 10.1007/BF00273016.
Unusual type of benign x-linked muscular dystrophy.
EMERY A, Dreifuss F
J Neurol Neurosurg Psychiatry. 1966; 29(4):338-42.
PMID: 5969090
PMC: 1064196.
DOI: 10.1136/jnnp.29.4.338.
[Contribution on the study of pseudohypertrophic muscular dystrophies. I. Benign pseudohypertrophic muscular dystrophy].
Radu H, Stenzel K
Dtsch Z Nervenheilkd. 1969; 196(2):92-115.
PMID: 5800957
