Evaluation of carrier detection rates for duchenne and becker muscular dystrophies using serum creatine-kinase(CK) and pyruvate-kinase(PK) through discriminant analysis-Reference-Cited by-同舟云学术

Evaluation of carrier detection rates for duchenne and becker muscular dystrophies using serum creatine-kinase(CK) and pyruvate-kinase(PK) through discriminant analysis

Published:1986-10 Issue:2 Volume:25 Page:219-230
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Zatz Mayana,Otto Paulo A.,Reynolds James F.

Publisher

Wiley

Subject

Genetics (clinical)

Reference13 articles.

1. Serum pyruvate kinase in muscle disease and carrier states

2. PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPs

3. DNA PROBES IN DUCHENNE MUSCULAR DYSTROPHY

4. BIRTH WEIGHT AND GESTATION TIME IN RELATION TO MATERNAL AGE, PARITY AND INFANT SURVIVAL

5. SOME NOTES ON DISCRIMINATION

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1. Sarcolemmal distribution of abnormal dystrophin in Xp21 carriers;Neuromuscular Disorders;1993-01

2. Screening of male patients with autosomal recessive Duchenne dystrophy through dystrophin and DNA studies;American Journal of Medical Genetics;1991-04-01

3. Estimate of the Intrafamilial Correlation for Serum Creatine Kinase and Pyruvate Kinase in Females at Risk for Duchenne and Becker Muscular Dystrophies;Human Heredity;1991

4. Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of Duchenne's and Becker muscular dystrophies of different ages;Neuromuscular Disorders;1991-01

5. Racial effect on serum creatine-kinase: Implications for estimation of heterozygosity risks for females at-risk for Duchenne dystrophy;Clinica Chimica Acta;1989-02