Results
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841.
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842.
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843.
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844.
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845.
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846.
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847.
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848.
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849.
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850.
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851.
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852.
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853.
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854.
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855.
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Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency). [electronic resource] by
- Schollen, E
- Frank, C G
- Keldermans, L
- Reyntjens, R
- Grubenmann, C E
- Clayton, P T
- Winchester, B G
- Smeitink, J
- Wevers, R A
- Aebi, M
- Hennet, T
- Matthijs, G
Producer: 20041221
In:
Journal of medical genetics vol. 41
Availability: No items available.
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856.
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857.
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858.
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859.
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860.
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A novel splice site mutation of the LDL receptor gene in a Tunisian hypercholesterolemic family. [electronic resource] by
- Jelassi, A
- Najah, M
- Jguirim, I
- Maatouk, F
- Lestavel, S
- Laroussi, O S
- Rouis, M
- Boileau, C
- Rabès, J P
- Varret, M
- Slimane, M N
Producer: 20080731
In:
Clinica chimica acta; international journal of clinical chemistry vol. 392
Availability: No items available.
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