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Identification of four novel mutations in patients with carnitine palmitoyltransferase II (CPT II) deficiency. [electronic resource] by
- Yang, B Z
- Ding, J H
- Dewese, T
- Roe, D
- He, G
- Wilkinson, J
- Day, D W
- Demaugre, F
- Rabier, D
- Brivet, M
- Roe, C
Producer: 19981125
In:
Molecular genetics and metabolism vol. 64
Availability: No items available.
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59.
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Chromosomal deletion 4p15.32----p14 in a Treacher Collins syndrome patient: exclusion of the disease locus from and mapping of anonymous DNA sequences to this region. [electronic resource] by
- Jabs, E W
- Coss, C A
- Hayflick, S J
- Whitmore, T E
- Pauli, R M
- Kirkpatrick, S J
- Meyers, D A
- Goldberg, R
- Day, D W
- Rosenbaum, K N
Producer: 19920214
In:
Genomics vol. 11
Availability: No items available.
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