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9201.
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Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation. [electronic resource] by
- Saitoh, S
- Buiting, K
- Cassidy, S B
- Conroy, J M
- Driscoll, D J
- Gabriel, J M
- Gillessen-Kaesbach, G
- Glenn, C C
- Greenswag, L R
- Horsthemke, B
- Kondo, I
- Kuwajima, K
- Niikawa, N
- Rogan, P K
- Schwartz, S
- Seip, J
- Williams, C A
- Nicholls, R D
Producer: 19970425
In:
American journal of medical genetics vol. 68
Availability: No items available.
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