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Search for mutations in pancreatic sufficient cystic fibrosis Italian patients: detection of 90% of molecular defects and identification of three novel mutations. [electronic resource] by
- Brancolini, V
- Cremonesi, L
- Belloni, E
- Pappalardo, E
- Bordoni, R
- Seia, M
- Russo, S
- Padoan, R
- Giunta, A
- Ferrari, M
Producer: 19950928
In:
Human genetics vol. 96
Availability: No items available.
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16.
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Immunochip analysis identifies novel susceptibility loci in the human leukocyte antigen region for acquired thrombotic thrombocytopenic purpura. [electronic resource] by
- Mancini, I
- Ricaño-Ponce, I
- Pappalardo, E
- Cairo, A
- Gorski, M M
- Casoli, G
- Ferrari, B
- Alberti, M
- Mikovic, D
- Noris, M
- Wijmenga, C
- Peyvandi, F
Producer: 20171225
In:
Journal of thrombosis and haemostasis : JTH vol. 14
Availability: No items available.
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17.
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Next-generation sequencing study finds an excess of rare, coding single-nucleotide variants of ADAMTS13 in patients with deep vein thrombosis. [electronic resource] by
- Lotta, L A
- Tuana, G
- Yu, J
- Martinelli, I
- Wang, M
- Yu, F
- Passamonti, S M
- Pappalardo, E
- Valsecchi, C
- Scherer, S E
- Hale, W
- Muzny, D M
- Randi, G
- Rosendaal, F R
- Gibbs, R A
- Peyvandi, F
Producer: 20140207
In:
Journal of thrombosis and haemostasis : JTH vol. 11
Availability: No items available.
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