Results
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26381.
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26382.
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26383.
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Molecular basis of fish-eye disease in a patient from Spain. Characterization of a novel mutation in the LCAT gene and lipid analysis of the cornea. [electronic resource] by
- Blanco-Vaca, F
- Qu, S J
- Fiol, C
- Fan, H Z
- Pao, Q
- Marzal-Casacuberta, A
- Albers, J J
- Hurtado, I
- Gracia, V
- Pintó, X
- Martí, T
- Pownall, H J
Producer: 19970904
In:
Arteriosclerosis, thrombosis, and vascular biology vol. 17
Availability: No items available.
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26384.
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26385.
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26386.
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26387.
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26388.
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26389.
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26390.
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26391.
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26392.
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26393.
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Sporadic imprinting defects in Prader-Willi syndrome and Angelman syndrome: implications for imprint-switch models, genetic counseling, and prenatal diagnosis. [electronic resource] by
- Buiting, K
- Dittrich, B
- Gross, S
- Lich, C
- Färber, C
- Buchholz, T
- Smith, E
- Reis, A
- Bürger, J
- Nöthen, M M
- Barth-Witte, U
- Janssen, B
- Abeliovich, D
- Lerer, I
- van den Ouweland, A M
- Halley, D J
- Schrander-Stumpel, C
- Smeets, H
- Meinecke, P
- Malcolm, S
- Gardner, A
- Lalande, M
- Nicholls, R D
- Friend, K
- Schulze, A
- Matthijs, G
- Kokkonen, H
- Hilbert, P
- Van Maldergem, L
- Glover, G
- Carbonell, P
- Willems, P
- Gillessen-Kaesbach, G
- Horsthemke, B
Producer: 19980813
In:
American journal of human genetics vol. 63
Availability: No items available.
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26394.
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26395.
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26396.
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26397.
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26398.
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26399.
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26400.
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