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Twelve novel mutations in the tissue-nonspecific alkaline phosphatase gene (ALPL) in patients with various forms of hypophosphatasia. [electronic resource] by
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Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation. [electronic resource] by
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- Bonduelle, M
- Chung, W
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- Fahey, M C
- Garrett, C
- Gillerot, Y
- Gillessen-Kaesbach, G
- Giménez-Arnau, A
- Guzzetta, F
- Battaglia, D
- Heimdal, K
- Lissens, W
- Taub, E
- Van Maldergem, L
- Van Paesschen, W
- Wieczorek, D
- Wood, N W
- Boon, L
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Human genetics vol. 122
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- Limaye, Nisha
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- Garzon, M
- Bonduelle, M
- Chung, W
- Daras, M D
- Fahey, M C
- Garrett, C
- Gillerot, Y
- Gillessen-Kaesbach, G
- Giménez-Arnau, A
- Guzzetta, F
- Battaglia, D
- Heimdal, K
- Lissens, W
- Taub, E
- Van Maldergem, L
- Van Paesschen, W
- Wieczorek, D
- Wood, N W
- Boon, L
- Vikkula, M
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Human genetics vol. 122
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- Garzon, M
- Bonduelle, M
- Chung, W
- Daras, M D
- Fahey, M C
- Garrett, C
- Gillerot, Y
- Gillessen-Kaesbach, G
- Giménez-Arnau, A
- Guzzetta, F
- Battaglia, D
- Heimdal, K
- Lissens, W
- Taub, E
- Van Maldergem, L
- Van Paesschen, W
- Wieczorek, D
- Wood, N W
- Boon, L
- Vikkula, M
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Human genetics vol. 122
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- Van Regemorter, N
- Garzon, M
- Bonduelle, M
- Chung, W
- Daras, M D
- Fahey, M C
- Garrett, C
- Gillerot, Y
- Gillessen-Kaesbach, G
- Giménez-Arnau, A
- Guzzetta, F
- Battaglia, D
- Heimdal, K
- Lissens, W
- Taub, E
- Van Maldergem, L
- Van Paesschen, W
- Wieczorek, D
- Wood, N W
- Boon, L
- Vikkula, M
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Human genetics vol. 122
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- Limaye, Nisha
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- Van Regemorter, N
- Garzon, M
- Bonduelle, M
- Chung, W
- Daras, M D
- Fahey, M C
- Garrett, C
- Gillerot, Y
- Gillessen-Kaesbach, G
- Giménez-Arnau, A
- Guzzetta, F
- Battaglia, D
- Heimda, K
- Lissens, W
- Taub, E
- Van Maldergem, L
- Van Paesschen, W
- Wieczorek, D
- Wood, N W
- Boon, L
- Vikkula, M
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Human genetics vol. 122
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- Limaye, Nisha
- Revencu, N
- Van Regemorter, N
- Garzon, M
- Bonduelle, M
- Chung, W
- Daras, M D
- Fahey, M C
- Garrett, C
- Gillerot, Y
- Gillessen-Kaesbach, G
- Giménez-Arnau, A
- Guzzetta, F
- Battaglia, D
- Heimdal, K
- Lissens, W
- Taub, E
- Van Maldergem, L
- Van Paesschen, W
- Wieczorek, D
- Wood, N W
- Boon, L
- Vikkula, M
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Human genetics vol. 122
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- Limaye, Nisha
- Revencu, N
- Van Regemorter, N
- Garzon, M
- Bonduelle, M
- Chung, W
- Daras, M D
- Fahey, M C
- Garrett, C
- Gillerot, Y
- Gillessen-Kaesbach, G
- Giménez-Arnau, A
- Guzzetta, F
- Battaglia, D
- Heimdal, K
- Lissens, W
- Taub, E
- Van Maldergem, L
- Van Paesschen, W
- Wieczorek, D
- Wood, N W
- Boon, L
- Vikkula, M
Producer: 20080416
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Human genetics vol. 122
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Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation. [electronic resource] by
- Limaye, Nisha
- Revencu, N
- Van Regemorter, N
- Garzon, M
- Bonduelle, M
- Chung, W
- Daras, M D
- Fahey, M C
- Garrett, C
- Gillerot, Y
- Gillessen-Kaesbach, G
- Giménez-Arnau, A
- Guzzetta, F
- Battaglia, D
- Heimdal, K
- Lissens, W
- Taub, E
- Van Maldergem, L
- Van Paesschen, W
- Wieczorek, D
- Wood, N W
- Boon, L
- Vikkula, M
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Human genetics vol. 122
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Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation. [electronic resource] by
- Limaye, Nisha
- Revencu, N
- Van Regemorter, N
- Garzon, M
- Bonduelle, M
- Chung, W
- Daras, M D
- Fahey, M C
- Garrett, C
- Gillerot, Y
- Gillessen-Kaesbach, G
- Giménez-Arnau, A
- Guzzetta, F
- Battaglia, D
- Heimda, K
- Lissens, W
- Taub, E
- Van Maldergem, L
- Van Paesschen, W
- Wieczorek, D
- Wood, N W
- Boon, L
- Vikkula, M
Producer: 20080416
In:
Human genetics vol. 122
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Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation. [electronic resource] by
- Limaye, Nisha
- Revencu, N
- Van Regemorter, N
- Garzon, M
- Bonduelle, M
- Chung, W
- Daras, M D
- Fahey, M C
- Garrett, C
- Gillerot, Y
- Gillessen-Kaesbach, G
- Giménez-Arnau, A
- Guzzetta, F
- Battaglia, D
- Heimdal, K
- Lissens, W
- Taub, E
- Van Maldergem, L
- Van Paesschen, W
- Wieczorek, D
- Wood, N W
- Boon, L
- Vikkula, M
Producer: 20080416
In:
Human genetics vol. 122
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Novel human pathological mutations. Gene symbol: KRIT1. Disease: cerebral cavernous malformation. [electronic resource] by
- Limaye, Nisha
- Revencu, N
- Van Regemorter, N
- Garzon, M
- Bonduelle, M
- Chung, W
- Daras, M D
- Fahey, M C
- Garrett, C
- Gillerot, Y
- Gillessen-Kaesbach, G
- Giménez-Arnau, A
- Guzzetta, F
- Battaglia, D
- Heimdal, K
- Lissens, W
- Taub, E
- Van Maldergem, L
- Van Paesschen, W
- Wieczorek, D
- Wood, N W
- Boon, L
- Vikkula, M
Producer: 20080416
In:
Human genetics vol. 122
Availability: No items available.
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