Artikkelit - Selaus tekijän mukaan "Paavola P"
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Assignment of the locus for hydrolethalus syndrome to a highly restricted region on 11q23-25
Visapää I; Salonen R; Varilo T; Paavola P; Peltonen L
Am J Hum Genet : 4 (1999) -
Characterization of a novel gene, PNUTL2, on human chromosome 17q22-q23 and its exclusion as the Meckel syndrome gene
Paavola P; Horelli-Kuitunen N; Palotie A; Peltonen L
Genomics : 5 (1999) -
Clinical and genetic heterogeneity in Meckel syndrome
Paavola P; Salonen R; Baumer A; Schinzel A; Boyd P A; Gould S; Meusburger H; Tenconi R; Barnicoat A; Winter R; Peltonen L
Hum Genet (1997) -
Exclusion of the P75 neurotrophin receptor gene as a candidate gene for Meckel syndrome
Wartiovaara K; Paavola P; Suvonto P; Paulin L; Saarma M; Peltonen L; Sariola H
CLIN DYSMORPHOL : 6 (1997) -
High-resolution physical and genetic mapping of the critical region for Meckel syndrome and Mulibrey Namism genes on chromosome 17q22-23
Paavola P; Avela K; Horelli-Kuitunen N; Bärlund M; Kallioniemi A; de la Chapelle A; Palotie A; Lehesjoki AE; Peltonen L
Genome Res : 3 (1999) -
Seasonal variation of seclusion incidents from violent and suicidal acts in forensic psychiatric patients
Paavola P; Tiihonen J
INT J LAW PSYCHIATRY : Dec 4 (2009) -
The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24
Paavola P; Salonen R; Weissenbach J; Peltonen L
Nat Genet (1995)