E-LIB Suche - Ergebnisse für: Koillinen, H.

1

Association and Mutation Analyses of theIRF6Gene in Familie..:

Pegelow, M. ; Koillinen, H. ; Magnusson, M....
The Cleft Palate-Craniofacial Journal. 51 (2014) 1 - p. 49-55 , 2014

Link: https://doi.org/10.1597/..

2

Targeted oligonucleotide-selective sequencing of 101 genes ..:

Alastalo, T. ; Akinrinade, O. ; Ollila, L....
Heart, Lung and Circulation. 23 (2014) - p. e2 , 2014

Link: https://doi.org/10.1016/..

3

Five new cases of a recently described leukoencephalopathy ..:

Linnankivi, T. ; Lundbom, N. ; Autti, T....
Neurology. 63 (2004) 4 - p. 688-692 , 2004

Link: https://doi.org/10.1212/..

4

Elucidating the genetic architecture of Adams-Oliver syndro..:

Meester, JAN ; Sukalo, M ; Schroeder, KC...
issn:1059-7794. , 2018

Link: http://hdl.handle.net/11..

5

Elucidating the genetic architecture of Adams-Oliver syndro..:

Meester, JAN ; Sukalo, M ; Schröder, KC...
https://openaccess.sgul.ac.uk/id/eprint/109915/7/Meester_et_al-2018-Human_Mutation.pdf. , 2018

Link: https://openaccess.sgul...

6

A genome-wide scan of non-syndromic cleft palate only (CPO)..:

Koillinen, H ; Lahermo, P ; Rautio, J...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1735976. , 2005

Link: http://www.ncbi.nlm.nih...

7

Linkage and linkage disequilibrium searched for between non..:

Koillinen, H ; Ollikainen, V ; Rautio, J..
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1735498. , 2003

Link: http://www.ncbi.nlm.nih...

8

Genetic heterogeneity and exclusion of a modifying locus at..:

WONG, F. K ; KOILLINEN, H ; RAUTIO, J...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1734824. , 2001

Link: http://www.ncbi.nlm.nih...

9

PTCH1 isoform 1b is the major transcript in the development..:

Gielen, Robbert-Jan C. A. M. ; Reinders, Marieke G. H. C. ; Koillinen, Hannele K....
Journal of Human Genetics. 63 (2018) 9 - p. 965-969 , 2018

Link: https://doi.org/10.1038/..

10

PTCH1 isoform 1b is the major transcript in the development..:

Gielen, Robbert-Jan C. A. M ; Reinders, Marieke G. H. C ; Koillinen, Hannele K...
Gielen , R-J C A M , Reinders , M G H C , Koillinen , H K , Paulussen , A D C , Mosterd , K & van Geel , M 2018 , ' PTCH1 isoform 1b is the major transcript in the development of basal cell nevus syndrome ' , Journal of Human Genetics , vol. 63 , no. 9 , pp. 965-969 . https://doi.org/10.1038/s10038-018-0485-0. , 2018

Link: https://cris.maastrichtu..