12 results on '"Zerres, K."'
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2. Intelligence and cognitive function in children and adolescents with spinal muscular atrophy
3. Becker’s muscular dystrophy aggravating facioscapulohumeral muscular dystrophy – double trouble as an explanation for an atypical phenotype
4. G.O.5 A new autosomal dominant distal vacuolar myopathy associated with mutation of the nuclear matrix protein, matrin 3
5. Response to comments by J.S. Sieratzki and B. Woll: Cognitive function in children with spinal muscular atrophy
6. Spinal muscular atrophy—clinical and genetic correlations
7. Multipoint linkage mapping of the Emery-Dreifuss muscular dystrophy gene
8. Stable motor and lung function throughout pregnancy in a patient with infantile spinal muscular atrophy type II
9. Intelligence and cognitive function in children and adolescents with spinal muscular atrophy
10. 59th ENMC International Workshop: Spinal Muscular Atrophies: recent progress and revised diagnostic criteria 17-19 April 1998, Soestduinen, The Netherlands
11. P.I.5 Mutations in SIL1 cause Marinesco–Sjögren syndrome, a cerebellar ataxia with cataract and myopathy
12. N.P.4 06 Natural history of severe infantile spinal muscular atrophy – preliminary results of a pilot study
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