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13521.
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13522.
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13523.
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13524.
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A microdeletion of less than 250 kb, including the proximal part of the FMR-I gene and the fragile-X site, in a male with the clinical phenotype of fragile-X syndrome. [electronic resource] by
- Wöhrle, D
- Kotzot, D
- Hirst, M C
- Manca, A
- Korn, B
- Schmidt, A
- Barbi, G
- Rott, H D
- Poustka, A
- Davies, K E
Producer: 19920901
In:
American journal of human genetics vol. 51
Availability: No items available.
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13525.
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13526.
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13527.
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13528.
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13529.
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13530.
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13531.
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13532.
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13534.
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13535.
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13536.
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13537.
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13538.
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13539.
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13540.
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