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Identification of a novel mutation (p.Ile198Thr) in gene TYR in a Pakistani family with nonsyndromic oculocutaneous albinism. [electronic resource] by
- Shah, S A
- Din, S U
- Raheem, N
- Daud, S
- Mubeen, J
- Nadeem, A
- Tayyab, M
- Baloch, D M
- Babar, M E
- Ahmad, J
Producer: 20150204
In:
Clinical and experimental dermatology vol. 39
Availability: No items available.
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34.
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Mutational spectrum of the TYR and SLC45A2 genes in Pakistani families with oculocutaneous albinism, and potential founder effect of missense substitution (p.Arg77Gln) of tyrosinase. [electronic resource] by
- Shah, S A
- Raheem, N
- Daud, S
- Mubeen, J
- Shaikh, A A
- Baloch, A H
- Nadeem, A
- Tayyab, M
- Babar, M E
- Ahmad, J
Producer: 20160623
In:
Clinical and experimental dermatology vol. 40
Availability: No items available.
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