Results
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621.
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An autosomal recessive leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa maps to chromosome 17q24.2-25.3. [electronic resource] by
- Bouhouche, Ahmed
- Benomar, Ali
- Errguig, Leila
- Lachhab, Lamiae
- Bouslam, Naima
- Aasfara, Jehanne
- Sefiani, Sanaa
- Chabraoui, Layachi
- El Fahime, Elmostafa
- El Quessar, Abdeljalil
- Jiddane, Mohamed
- Yahyaoui, Mohamed
Producer: 20120627
In:
BMC medical genetics vol. 13
Availability: No items available.
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622.
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623.
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624.
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625.
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626.
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627.
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628.
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629.
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630.
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631.
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632.
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633.
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634.
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635.
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636.
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De novo unbalanced translocation 2;4 characterized by metaphase CGH and array CGH in a child with mental retardation and dysmorphic features. [electronic resource] by
- Debost-Legrand, A
- Capri, Y
- Gouas, L
- Pebrel-Richard, C
- Veronese, L
- Tchirkov, A
- Haoud, K
- Boespflug-Tanguy, O
- Goumy, C
- Vago, P
Producer: 20120501
In:
Pathologie-biologie vol. 59
Availability: No items available.
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637.
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638.
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639.
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640.
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