Suchergebnisse - "Bunyan, David J"

PubPharm (4)

1

Recurrence and variability of germline EPCAM deletions in Lynch syndrome

enthalten in: Human mutation | 2011

von Kuiper, R. | Vissers, L. | Venkatachalam, R. | +32

2

Recurrence and variability of germline EPCAM deletions in Lynch syndrome

enthalten in: Human mutation | 2011

von Kuiper, R. | Vissers, L. | Venkatachalam, R. | +32

3

Novel heterozygous OTX2 mutations and whole gene deletions in anophthalmia, microphthalmia and coloboma

enthalten in: Human mutation | 2008

von Wyatt, A. | Bakrania, P. | Bunyan, D. | +9

4

Novel heterozygous OTX2 mutations and whole gene deletions in anophthalmia, microphthalmia and colobomaCommunicated by Mark H. Paalman

enthalten in: Human mutation | 2008

von Wyatt, A. | Bakrania, P. | Bunyan, D. | +9

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