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Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization. [electronic resource] by
- Lindsay, E A
- Grillo, A
- Ferrero, G B
- Roth, E J
- Magenis, E
- Grompe, M
- Hultén, M
- Gould, C
- Baldini, A
- Zoghbi, H Y
Producer: 19940325
In:
American journal of medical genetics vol. 49
Availability: No items available.
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78.
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79.
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Identification and characterization of the gene causing type 1 spinocerebellar ataxia. [electronic resource] by
- Banfi, S
- Servadio, A
- Chung, M Y
- Kwiatkowski, T J
- McCall, A E
- Duvick, L A
- Shen, Y
- Roth, E J
- Orr, H T
- Zoghbi, H Y
Producer: 19941229
In:
Nature genetics vol. 7
Availability: No items available.
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80.
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Yeast artificial chromosome cloning in the glycerol kinase and adrenal hypoplasia congenita region of Xp21. [electronic resource] by
- Worley, K C
- Ellison, K A
- Zhang, Y H
- Wang, D F
- Mason, J
- Roth, E J
- Adams, V
- Fogt, D D
- Zhu, X M
- Towbin, J A
Producer: 19930726
In:
Genomics vol. 16
Availability: No items available.
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