Results
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8021.
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8022.
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8023.
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8024.
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8025.
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8026.
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8027.
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8028.
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8029.
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8030.
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8031.
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8032.
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8033.
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8034.
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8035.
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Molecular characterization of 3-phosphoglycerate dehydrogenase deficiency--a neurometabolic disorder associated with reduced L-serine biosynthesis. [electronic resource] by
- Klomp, L W
- de Koning, T J
- Malingré, H E
- van Beurden, E A
- Brink, M
- Opdam, F L
- Duran, M
- Jaeken, J
- Pineda, M
- Van Maldergem, L
- Poll-The, B T
- van den Berg, I E
- Berger, R
Producer: 20010118
In:
American journal of human genetics vol. 67
Availability: No items available.
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8036.
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Distinct missense mutations of the FGFR3 lys650 codon modulate receptor kinase activation and the severity of the skeletal dysplasia phenotype. [electronic resource] by
- Bellus, G A
- Spector, E B
- Speiser, P W
- Weaver, C A
- Garber, A T
- Bryke, C R
- Israel, J
- Rosengren, S S
- Webster, M K
- Donoghue, D J
- Francomano, C A
Producer: 20010118
In:
American journal of human genetics vol. 67
Availability: No items available.
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8037.
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8038.
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8039.
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8040.
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