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34.
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Cloning of the esterase D gene: a polymorphic gene probe closely linked to the retinoblastoma locus on chromosome 13. [electronic resource] by
- Squire, J
- Dryja, T P
- Dunn, J
- Goddard, A
- Hofmann, T
- Musarella, M
- Willard, H F
- Becker, A J
- Gallie, B L
- Phillips, R A
Producer: 19861003
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 83
Availability: No items available.
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35.
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Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3. [electronic resource] by
- Musarella, M A
- Weleber, R G
- Murphey, W H
- Young, R S
- Anson-Cartwright, L
- Mets, M
- Kraft, S P
- Polemeno, R
- Litt, M
- Worton, R G
Producer: 19900125
In:
Genomics vol. 5
Availability: No items available.
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38.
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Mutations in MKKS cause Bardet-Biedl syndrome. [electronic resource] by
- Slavotinek, A M
- Stone, E M
- Mykytyn, K
- Heckenlively, J R
- Green, J S
- Heon, E
- Musarella, M A
- Parfrey, P S
- Sheffield, V C
- Biesecker, L G
Producer: 20001030
In:
Nature genetics vol. 26
Availability: No items available.
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39.
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Dystrophin expression in the human retina is required for normal function as defined by electroretinography. [electronic resource] by
- Pillers, D A
- Bulman, D E
- Weleber, R G
- Sigesmund, D A
- Musarella, M A
- Powell, B R
- Murphey, W H
- Westall, C
- Panton, C
- Becker, L E
Producer: 19930719
In:
Nature genetics vol. 4
Availability: No items available.
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40.
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Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophy. [electronic resource] by
- Sigesmund, D A
- Weleber, R G
- Pillers, D A
- Westall, C A
- Panton, C M
- Powell, B R
- Héon, E
- Murphey, W H
- Musarella, M A
- Ray, P N
Producer: 19940620
In:
Ophthalmology vol. 101
Availability: No items available.
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