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Biotinidase deficiency: novel mutations in Algerian patients. [electronic resource] by
- Tiar, A
- Mekki, A
- Nagara, M
- Rhouma, F Ben
- Messaoud, O
- Halim, N Ben
- Kefi, R
- Hamlaoui, M T
- Lebied, A
- Abdelhak, S
Producer: 20140304
In:
Gene vol. 536
Availability: No items available.
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18.
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[Antiphospholipid antibodies in 146 women with repeated pregnancy losses]. [electronic resource] by
- Ben Hadj Slama, F
- Nagara, M
- Slama, A
- Braham Jmili, N
- Monastiri, K
- Laouani-Kechrid, C
- Toumi, N H
- N'Siri, B
- Samama, M
- Mahjoub, T
Producer: 20040830
In:
Annales de biologie clinique vol. 62
Availability: No items available.
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19.
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Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasia. [electronic resource] by
- Zanni, G
- Saillour, Y
- Nagara, M
- Billuart, P
- Castelnau, L
- Moraine, C
- Faivre, L
- Bertini, E
- Durr, A
- Guichet, A
- Rodriguez, D
- des Portes, V
- Beldjord, C
- Chelly, J
Producer: 20060412
In:
Neurology vol. 65
Availability: No items available.
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20.
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Clinical, genealogical and molecular investigation of the xeroderma pigmentosum type C complementation group in Tunisia. [electronic resource] by
- Jerbi, M
- Ben Rekaya, M
- Naouali, C
- Jones, M
- Messaoud, O
- Tounsi, H
- Nagara, M
- Chargui, M
- Kefi, R
- Boussen, H
- Mokni, M
- Mrad, R
- Boubaker, M S
- Abdelhak, S
- Khaled, A
- Zghal, M
- Yacoub-Youssef, H
Producer: 20161214
In:
The British journal of dermatology vol. 174
Availability: No items available.
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