- R, Kivitie-Kallio S,
Norio R,
Warburg M,
Fryns JP, de la
Chapelle A,
Lehesjoki AE (June 2003). "Cohen
syndrome is
caused by
mutations in a
novel gene...
- MCY; Mancini, GMS; Sztriha, L; Im, K; Amrom, D; Andermann, E; Paetau, R;
Lehesjoki, AE; Walsh, CA; Lehtinen, MK (5
September 2018). "Sodium
Channel SCN3A...
- R, Kivitie-Kallio S,
Norio R,
Warburg M,
Fryns JP, de la
Chapelle A,
Lehesjoki AE (June 2003). "Cohen syndrome".
American Journal of
Human Genetics....
- C,
Dugan SL, Vainionpää L,
Karle KN,
Synofzik M, Schöls L, Schüle R,
Lehesjoki AE,
Helbig I,
Lerche H,
Lemke JR (2016) A
recurrent mutation in KCNA2...
- JB,
Willour V,
Pennacchio LA,
Warrington JA, Hu A, de la
Chapelle A,
Lehesjoki AE, Cox DR,
Myers RM (March 1996). "Construction of a 750-kb bacterial...
- doi:10.1093/hmg/8.10.1913. PMID 10469845. de la
Chapelle A, Hästbacka J,
Lehesjoki AE,
Sulisalo T, Kere J,
Tahvanainen E,
Sistonen P (1994). "[Linkage and...
-
muscle involvement in
dynamin 2-related
centronuclear myopathy". Brain.
Lehesjoki A,
Sankila E, Miao J,
Somer M,
Salonen R,
Rapola J, de la
Chapelle A (1990)...
- (9): 2140–51. doi:10.1093/emboj/20.9.2140. PMC 125245. PMID 11331580.
Lehesjoki AE, Reed VA, Mark
Gardiner R,
Greene ND (October 2001). "Expression of...
-
Soares MB,
Bonaldo MF,
Hirvasniemi A, de la
Chapelle A,
Gilliam TC,
Lehesjoki AE (Oct 1999). "The
neuronal ceroid lipofuscinoses in
human EPMR and mnd...
- 702H. doi:10.1038/31508. PMID 9641683. S2CID 205001265.
Pennacchio LA,
Lehesjoki AE,
Stone NE,
Willour VL,
Virtaneva K, Miao J, et al. (March 1996). "Mutations...
