J. Tallila
发表
Päivi Heikkilä,
Jiri Bartek,
Nazneen Rahman,
2006,
International journal of cancer.
M. Gentile,
T. Heliö,
S. Tuupanen,
2021,
BMC Cardiovascular Disorders.
M. Irving,
J. Koskenvuo,
L. Pelttari,
2021,
Orphanet Journal of Rare Diseases.
L. Peltonen,
R. Salonen,
M. Kestilä,
2009,
Human mutation.
Identification of CC2D2A as a Meckel syndrome gene adds an important piece to the ciliopathy puzzle.
L. Peltonen,
R. Salonen,
E. Jakkula,
2008,
American journal of human genetics.
S. Myllykangas,
J. Koskenvuo,
T. Alastalo,
2015,
American journal of medical genetics. Part A.
R. Salonen,
M. Gentile,
T. Varilo,
2010,
The New England journal of medicine.
B. Popescu,
A. Bastian,
B. Popescu,
2017,
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie.
R. Salonen,
M. Gentile,
T. Varilo,
2010
.
Päivi Heikkilä,
Heli Nevanlinna,
Kristiina Aittomäki,
2005,
Clinical Cancer Research.
Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders
M. Jarvelin,
M. Daly,
K. Kristiansson,
2013,
Nature Neuroscience.
M. Gentile,
S. Myllykangas,
J. Koskenvuo,
2015,
Molecular genetics & genomic medicine.
J. Tallila,
2009
.
C. Vasilescu,
A. Paetau,
T. Ojala,
2016,
American journal of medical genetics. Part A.
Berthold Göttgens,
Nicole Soranzo,
Suthesh Sivapalaratnam,
2011,
PLoS genetics.
L. Peltonen,
R. Salonen,
M. Kestilä,
2006,
Nature Genetics.
L. Peltonen,
N. Pakkasjärvi,
Satu Kuure,
2008,
Nature Genetics.
C. Vasilescu,
T. Ojala,
T. Heliö,
2015,
Journal of Cardiovascular Magnetic Resonance.
M. Nieminen,
M. Gentile,
M. Kaartinen,
2015,
European heart journal.
M. Irving,
J. Koskenvuo,
L. Pelttari,
2021,
Orphanet Journal of Rare Diseases.
S. Myllykangas,
J. Koskenvuo,
T. Alastalo,
2014
.
M. Irving,
J. Koskenvuo,
T. Kangas-Kontio,
2022,
Orphanet Journal of Rare Diseases.