CLINICAL MANIFESTATIONS IN TWO CARRIERS OF DUCHENNE MUSCULAR DYSTROPHY-Reference-Cited by-同舟云学术

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CLINICAL MANIFESTATIONS IN TWO CARRIERS OF DUCHENNE MUSCULAR DYSTROPHY

Published:1963-05 Issue:7291 Volume:281 Page:1126-1128
ISSN:0140-6736
Container-title:The Lancet
language:en
Short-container-title:The Lancet

Author:

Emery AlanE.H.

Publisher

Elsevier BV

Subject

General Medicine

Reference18 articles.

1. Diseases of Muscle;Adams,1962

2. THE NORMAL HUMAN FEMALE AS A MOSAIC OF X-CHROMOSOME ACTIVITY: STUDIES USING THE GENE FOR G-6-PD-DEFICIENCY AS A MARKER

3. Biochemistry of Hereditary Myopathies;Dreyfus,1962

Cited by 63 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. CARRIER DETECTION AND GENETIC COUNSELLING IN DUCHENNE DYSTROPHY;Developmental Medicine & Child Neurology;2008-11-12

2. Carrier detection in Duchenne muscular dystrophy using computed tomography;Clinical Genetics;2008-06-28

3. Clinically manifesting carriers in Duchenne muscular dystrophy;Clinical Genetics;2008-04-23

4. STUDIES ON HUMAN MUSCULAR DYSTROPHY WITH PARTICULAR REFERENCE TO METHODS OF CARRIER DETECTION;Annals of the New York Academy of Sciences;2006-12-16

5. Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers;American Journal of Medical Genetics;1998-12-04

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