Results
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17021.
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17022.
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17023.
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17024.
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17025.
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Clinical homogeneity of the Stüve-Wiedemann syndrome and overlap with the Schwartz-Jampel syndrome type 2. [electronic resource] by
- Cormier-Daire, V
- Superti-Furga, A
- Munnich, A
- Lyonnet, S
- Rustin, P
- Delezoide, A L
- De Lonlay, P
- Giedion, A
- Maroteaux, P
- Le Merrer, M
Producer: 19980924
In:
American journal of medical genetics vol. 78
Availability: No items available.
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17026.
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17027.
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17028.
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Clinical and haematological consequences of recurrent G6PD mutations and a single new mutation causing chronic nonspherocytic haemolytic anaemia. [electronic resource] by
- Vulliamy, T J
- Kaeda, J S
- Ait-Chafa, D
- Mangerini, R
- Roper, D
- Barbot, J
- Mehta, A B
- Athanassiou-Metaxa, M
- Luzzatto, L
- Mason, P J
Producer: 19980805
In:
British journal of haematology vol. 101
Availability: No items available.
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17029.
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17030.
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17031.
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17032.
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17033.
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17034.
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17035.
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17036.
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17037.
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17038.
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17039.
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17040.
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