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A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism
- Koolen, DA (author)
- Vissers, LELM (author)
- Pfundt, R (author)
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- de Leeuw, N (author)
- Knight, SJL (author)
- Regan, R (author)
- Kooy, RF (author)
- Reyniers, E (author)
- Romano, C (author)
- Fichera, M (author)
- Schinzel, A (author)
- Baumer, A (author)
- Knoers, NV (author)
- van Kessel, AG (author)
- Sistermans, EA (author)
- Veltman, JA (author)
- Brunner, HG (author)
- de Vries, BBA (author)
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- (creator_code:org_t)
- 2006-08-13
- 2006
- English.
- In: Nature genetics. - : Springer Science and Business Media LLC. - 1061-4036 .- 1546-1718. ; 38:9, s. 999-1001
- Journal article (peer-reviewed)
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- Koolen, DA
- Vissers, LELM
- Pfundt, R
- de Leeuw, N
- Knight, SJL
- Regan, R
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- Kooy, RF
- Reyniers, E
- Romano, C
- Fichera, M
- Schinzel, A
- Baumer, A
- Anderlid, BM
- Schoumans, J
- Knoers, NV
- van Kessel, AG
- Sistermans, EA
- Veltman, JA
- Brunner, HG
- de Vries, BBA
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- Nature genetics
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- Karolinska Institutet
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