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54.
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Chromosome 2 deletion encompassing the MAP2 gene in a patient with autism and Rett-like features. [electronic resource] by
- Pescucci, C
- Meloni, I
- Bruttini, M
- Ariani, F
- Longo, I
- Mari, F
- Canitano, R
- Hayek, G
- Zappella, M
- Renieri, A
Producer: 20040720
In:
Clinical genetics vol. 64
Availability: No items available.
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55.
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Preserved speech variant is allelic of classic Rett syndrome. [electronic resource] by
- De Bona, C
- Zappella, M
- Hayek, G
- Meloni, I
- Vitelli, F
- Bruttini, M
- Cusano, R
- Loffredo, P
- Longo, I
- Renieri, A
Producer: 20000918
In:
European journal of human genetics : EJHG vol. 8
Availability: No items available.
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56.
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MECP2 mutation in male patients with non-specific X-linked mental retardation. [electronic resource] by
- Orrico, A
- Lam, C
- Galli, L
- Dotti, M T
- Hayek, G
- Tong, S F
- Poon, P M
- Zappella, M
- Federico, A
- Sorrentino, V
Producer: 20001018
In:
FEBS letters vol. 481
Availability: No items available.
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57.
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Dual X-ray absorptiometry and bone ultrasonography in patients with Rett syndrome. [electronic resource] by
- Cepollaro, C
- Gonnelli, S
- Bruni, D
- Pacini, S
- Martini, S
- Franci, M B
- Gennari, L
- Rossi, S
- Hayek, G
- Zappella, M
- Gennari, C
Producer: 20020607
In:
Calcified tissue international vol. 69
Availability: No items available.
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58.
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Neurocutaneous syndrome with mental delay, autism, blockage in intracellular vescicular trafficking and melanosome defects. [electronic resource] by
- Buoni, S
- Zannolli, R
- de Santi, M
- Macucci, F
- Hayek, J
- Orsi, A
- Scarinci, R
- Buscalferri, A
- Cuccia, A
- Zappella, M
- Miracco, C
Producer: 20060830
In:
European journal of neurology vol. 13
Availability: No items available.
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59.
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Diagnostic criteria for the Zappella variant of Rett syndrome (the preserved speech variant). [electronic resource] by
- Renieri, A
- Mari, F
- Mencarelli, M A
- Scala, E
- Ariani, F
- Longo, I
- Meloni, I
- Cevenini, G
- Pini, G
- Hayek, G
- Zappella, M
Producer: 20090313
In:
Brain & development vol. 31
Availability: No items available.
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60.
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CDKL5/STK9 is mutated in Rett syndrome variant with infantile spasms. [electronic resource] by
- Scala, E
- Ariani, F
- Mari, F
- Caselli, R
- Pescucci, C
- Longo, I
- Meloni, I
- Giachino, D
- Bruttini, M
- Hayek, G
- Zappella, M
- Renieri, A
Producer: 20060420
In:
Journal of medical genetics vol. 42
Availability: No items available.
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