Myopathy in a patient with chromosome 22q11 deletion. [electronic resource]
Producer: 20011204Description: 107-9 p. digitalISSN:- 0174-304X
- Abnormalities, Multiple -- diagnosis
- Adolescent
- Biopsy
- Chromosome Deletion
- Chromosomes, Human, Pair 22
- Craniofacial Abnormalities -- diagnosis
- Creatine Kinase -- blood
- Glycogen -- metabolism
- Humans
- Male
- Microscopy, Electron
- Muscle, Skeletal -- pathology
- Muscular Atrophy -- diagnosis
- Neuromuscular Diseases -- diagnosis
No physical items for this record
Publication Type: Case Reports; Letter; Research Support, Non-U.S. Gov't
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