Results
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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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3.
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Mapping of the familial infantile myasthenia (congenital myasthenic syndrome type Ia) gene to chromosome 17p with evidence of genetic homogeneity. [electronic resource] by
- Christodoulou, K
- Tsingis, M
- Deymeer, F
- Serdaroglu, P
- Ozdemir, C
- Al-Shehab, A
- Bairactaris, C
- Mavromatis, I
- Mylonas, I
- Evoli, A
- Kyriallis, K
- Middleton, L T
Producer: 19970715
In:
Human molecular genetics vol. 6
Availability: No items available.
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4.
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A novel form of distal hereditary motor neuronopathy maps to chromosome 9p21.1-p12. [electronic resource] by
- Christodoulou, K
- Zamba, E
- Tsingis, M
- Mubaidin, A
- Horani, K
- Abu-Sheik, S
- El-Khateeb, M
- Kyriacou, K
- Kyriakides, T
- Al-Qudah, A K
- Middleton, L
Producer: 20010111
In:
Annals of neurology vol. 48
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-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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6.
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Congenital myasthenic syndrome. (CMS) type Ia. Clinical and genetic diversity. [electronic resource] by
- Middleton, L T
- Christodoulou, K
- Deymeer, F
- Serdaroglu, P
- Ozdemir, C
- al-Qudah, A K
- al-Shehab, A
- Mavromatis, I
- Mylonas, I
- Evoli, A
- Tsingis, M
- Zamba, E
- Kyriallis, K
Producer: 19980804
In:
Annals of the New York Academy of Sciences vol. 841
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-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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8.
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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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9.
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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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10.
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Chromosome 17p-linked myasthenias stem from defects in the acetylcholine receptor epsilon-subunit gene. [electronic resource] by
- Middleton, L
- Ohno, K
- Christodoulou, K
- Brengman, J
- Milone, M
- Neocleous, V
- Serdaroğlu, P
- Deymeer, F
- Ozdemir, C
- Mubaidin, A
- Horany, K
- Al-Shehab, A
- Mavromatis, I
- Mylonas, I
- Tsingis, M
- Zamba, E
- Pantzaris, M
- Kyriallis, K
- Engel, A G
Producer: 19991115
In:
Neurology vol. 53
Availability: No items available.
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