Results
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273.
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Two de novo GJA1 mutation in two sporadic patients with erythrokeratodermia variabilis et progressiva. [electronic resource] by
- Li, Changxing
- Liang, Jingyao
- Chen, Pingjiao
- Zeng, Kang
- Xue, Rujun
- Tian, Xin
- Liang, Liuping
- Wang, Qi
- Shi, Minglan
- Zhang, Xibao
Producer: 20200623
In:
Molecular genetics & genomic medicine vol. 7
Availability: No items available.
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274.
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275.
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276.
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277.
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278.
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279.
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280.
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GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype. [electronic resource] by
- Paznekas, William A
- Karczeski, Barbara
- Vermeer, Sascha
- Lowry, R Brian
- Delatycki, Martin
- Laurence, Faivre
- Koivisto, Pasi A
- Van Maldergem, Lionel
- Boyadjiev, Simeon A
- Bodurtha, Joann N
- Jabs, Ethylin Wang
Producer: 20090730
In:
Human mutation vol. 30
Availability: No items available.
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