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Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene. [electronic resource] by
- Broughton, B C
- Berneburg, M
- Fawcett, H
- Taylor, E M
- Arlett, C F
- Nardo, T
- Stefanini, M
- Menefee, E
- Price, V H
- Queille, S
- Sarasin, A
- Bohnert, E
- Krutmann, J
- Davidson, R
- Kraemer, K H
- Lehmann, A R
Producer: 20020221
In:
Human molecular genetics vol. 10
Availability: No items available.
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