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Mapping of the second Friedreich's ataxia (FRDA2) locus to chromosome 9p23-p11: evidence for further locus heterogeneity. [electronic resource] by
- Christodoulou, K
- Deymeer, F
- Serdaroğlu, P
- Ozdemir, C
- Poda, M
- Georgiou, D M
- Ioannou, P
- Tsingis, M
- Zamba, E
- Middleton, L T
Producer: 20020116
In:
Neurogenetics vol. 3
Availability: No items available.
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4.
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Distal hereditary motor neuronopathy of the Jerash type. [electronic resource] by
- Middleton, L T
- Christodoulou, K
- Mubaidin, A
- Zamba, E
- Tsingis, M
- Kyriacou, K
- Abu-Sheikh, S
- Kyriakides, T
- Neocleous, V
- Georgiou, D M
- el-Khateeb, M
- al-Qudah, A
- Horany, K
Producer: 19991221
In:
Annals of the New York Academy of Sciences vol. 883
Availability: No items available.
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5.
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Distal Hereditary Motor Neuronopathy of the Jerash Type. [electronic resource] by
- Middleton, L T
- Christodoulou, K
- Mubaidin, A
- Zamba, E
- Tsingis, M
- Kyriacou, K
- Abu-Sheikh, S
- Kyriakides, T
- Neocleous, V
- Georgiou, D M
- El-Khateeb, M
- Al-Qudan, A
- Horany, K
Publication details: Annals of the New York Academy of Sciences Oct 1999
In:
Annals of the New York Academy of Sciences vol. 883
Availability: No items available.
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6.
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Distal hereditary motor neuronopathy of the Jerash type. [electronic resource] by
- Middleton, L T
- Christodoulou, K
- Mubaidin, A
- Zamba, E
- Tsingis, M
- Kyriacou, K
- Abu-Sheikh, S
- Kyriakides, T
- Neocleous, V
- Georgiou, D M
- el-Khateeb, M
- al-Qudah, A
- Horany, K
Producer: 19991221
In:
Annals of the New York Academy of Sciences vol. 883
Availability: No items available.
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7.
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Distal Hereditary Motor Neuronopathy of the Jerash Type. [electronic resource] by
- Middleton, L T
- Christodoulou, K
- Mubaidin, A
- Zamba, E
- Tsingis, M
- Kyriacou, K
- Abu-Sheikh, S
- Kyriakides, T
- Neocleous, V
- Georgiou, D M
- El-Khateeb, M
- Al-Qudah, A
- Horany, K
Publication details: Annals of the New York Academy of Sciences Oct 1999
In:
Annals of the New York Academy of Sciences vol. 883
Availability: No items available.
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8.
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Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2. [electronic resource] by
- Bolino, A
- Muglia, M
- Conforti, F L
- LeGuern, E
- Salih, M A
- Georgiou, D M
- Christodoulou, K
- Hausmanowa-Petrusewicz, I
- Mandich, P
- Schenone, A
- Gambardella, A
- Bono, F
- Quattrone, A
- Devoto, M
- Monaco, A P
Producer: 20000612
In:
Nature genetics vol. 25
Availability: No items available.
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9.
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Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22. [electronic resource] by
- Bolino, A
- Levy, E R
- Muglia, M
- Conforti, F L
- LeGuern, E
- Salih, M A
- Georgiou, D M
- Christodoulou, R K
- Hausmanowa-Petrusewicz, I
- Mandich, P
- Gambardella, A
- Quattrone, A
- Devoto, M
- Monaco, A P
Producer: 20000418
In:
Genomics vol. 63
Availability: No items available.
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