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Familial 1.1 Mb deletion in chromosome Xq22.1 associated with mental retardation and behavioural disorders in female patients. [electronic resource] by
- Grillo, L
- Reitano, S
- Belfiore, G
- Spalletta, A
- Amata, S
- Bottitta, M
- Barone, C
- Falco, M
- Fichera, M
- Romano, C
Producer: 20100714
In:
European journal of medical genetics vol. 53
Availability: No items available.
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39.
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New mutations in XNP/ATR-X gene: a further contribution to genotype/phenotype relationship in ATR/X syndrome. Mutations in brief no. 176. Online. [electronic resource] by
- Fichera, M
- Romano, C
- Castiglia, L
- Failla, P
- Ruberto, C
- Amata, S
- Greco, D
- Cardoso, C
- Fontés, M
- Ragusa, A
Producer: 20000201
In:
Human mutation vol. 12
Availability: No items available.
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40.
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Schizophrenia in a patient with subtelomeric duplication of chromosome 22q. [electronic resource] by
- Failla, P
- Romano, C
- Alberti, A
- Vasta, A
- Buono, S
- Castiglia, L
- Luciano, D
- Di Benedetto, D
- Fichera, M
- Galesi, O
Producer: 20070730
In:
Clinical genetics vol. 71
Availability: No items available.
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