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A deletion including the brain promoter of the Duchenne muscular dystrophy gene is not associated with mental retardation. [electronic resource] by
- Rapaport, D
- Passos-Bueno, M R
- Takata, R I
- Campiotto, S
- Eggers, S
- Vainzof, M
- Makover, A
- Nudel, U
- Yaffe, D
- Zatz, M
Producer: 19921207
In:
Neuromuscular disorders : NMD vol. 2
Availability: No items available.
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Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation? [electronic resource] by
- Passos-Bueno, M R
- Byth, B C
- Rosenberg, S
- Takata, R I
- Bakker, E
- Beggs, A H
- Pavanello, R C
- Vainzof, M
- Davies, K E
- Zatz, M
Producer: 19930601
In:
American journal of medical genetics vol. 46
Availability: No items available.
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Clinical diagnosis of heterozygous dystrophin gene deletions by fluorescence in situ hybridization. [electronic resource] by
- Rosenberg, C
- Navajas, L
- Vagenas, D F
- Bakker, E
- Vainzof, M
- Passos-Bueno, M R
- Takata, R I
- Van Ommen, G J
- Zatz, M
- Den Dunnen, J T
Producer: 19990204
In:
Neuromuscular disorders : NMD vol. 8
Availability: No items available.
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A new locus for recessive distal spinal muscular atrophy at Xq13.1-q21. [electronic resource] by
- Takata, R I
- Speck Martins, C E
- Passosbueno, M R
- Abe, K T
- Nishimura, A L
- Da Silva, M Dorvalina
- Monteiro, A
- Lima, M I
- Kok, F
- Zatz, M
Producer: 20040615
In:
Journal of medical genetics vol. 41
Availability: No items available.
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