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Correction to: Structural modeling of a novel TERC variant in a patient with aplastic anemia and short telomeres. [electronic resource] by
- Rinelli, M
- Bellacchio, E
- Berardinelli, F
- Pascolini, G
- Grammatico, P
- Sgura, A
- Iori, A P
- Quattrocchi, L
- Novelli, A
- Majore, S
- Agolini, E
Publication details: Annals of hematology 03 2019
In:
Annals of hematology vol. 98
Availability: No items available.
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Structural modeling of a novel TERC variant in a patient with aplastic anemia and short telomeres. [electronic resource] by
- Rinelli, M
- Bellacchio, E
- Berardinelli, F
- Pascolini, G
- Grammatico, P
- Sgura, A
- Iori, A P
- Quattrocchi, L
- Novelli, A
- Majore, S
- Agolini, E
Producer: 20190225
In:
Annals of hematology vol. 98
Availability: No items available.
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6.
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Expanding the clinical and molecular spectrum of PRMT7 mutations: 3 additional patients and review. [electronic resource] by
- Agolini, E
- Dentici, M L
- Bellacchio, E
- Alesi, V
- Radio, F C
- Torella, A
- Musacchia, F
- Tartaglia, M
- Dallapiccola, B
- Nigro, V
- Digilio, M C
- Novelli, A
Producer: 20190911
In:
Clinical genetics vol. 93
Availability: No items available.
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Novel homozygous mutation in exon 5 of WFS1 gene in an Apulian family with mild phenotypic expression of Wolfram syndrome. [electronic resource] by
- Piccinno, E
- Ortolani, F
- Vendemiale, M
- Tummolo, A
- Masciopinto, M
- Natale, M P
- De Luca, A
- Agolini, E
- Aloi, C
- Salina, A
- D'Annunzio, G
- Fischetto, R
- Papadia, F
Producer: 20150312
In:
Clinical genetics vol. 86
Availability: No items available.
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