Polycystic kidney disease in children: a genetic and epidemiological study of 82 Finnish patients.

Por Kääriäinen, H
Publicado em 1987

Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.

Por Lindlöf, M, Kääriäinen, H, Davies, K E, de la Chapelle, A
Publicado em 1986

Clinical features of nine males with molecularly defined deletions of the Y chromosome long arm.

Por Salo, P, Ignatius, J, Simola, K O, Tahvanainen, E, Kääriäinen, H
Publicado em 1995

Comprehension of cancer risk one and 12 months after predictive genetic testing for hereditary non-polyposis colorectal cancer

Por Aktan-Collan, K., Haukkala, A., Mecklin, J., Uutela, A., Kaariainen, H.
Publicado em 2001

Genetics of congenital nemaline myopathy: a study of 10 families.

Por Wallgren-Pettersson, C, Kääriäinen, H, Rapola, J, Salmi, T, Jääskeläinen, J, Donner, M
Publicado em 1990

Molecular studies in Finnish patients with familial juvenile nephronophthisis exclude a founder effect and support a common mutation causing mechanism.

Por Ala-Mello, S, Sankila, E M, Koskimies, O, de la Chapelle, A, Kääriäinen, H
Publicado em 1998

Carrier testing of children for two X linked diseases in a family based setting: a retrospective long term psychosocial evaluation

Por Jarvinen, O., Aalto, A., Lehesjoki, A., Lindlof, M., Soderling, I., Uutela, A., Kaariainen, H.
Publicado em 1999

Evaluation of a counselling protocol for predictive genetic testing for hereditary non-polyposis colorectal cancer

Por Aktan-Collan, K., Mecklin, J., de la Chapelle, A., Peltomaki, P., Uutela, A., Kaariainen, H.
Publicado em 2000

Mutation in type II procollagen (COL2A1) that substitutes aspartate for glycine alpha 1-67 and that causes cataracts and retinal detachment: evidence for molecular heterogeneity in...

Por Körkkö, J, Ritvaniemi, P, Haataja, L, Kääriäinen, H, Kivirikko, K I, Prockop, D J, Ala-Kokko, L
Publicado em 1993

ATM mutations in Finnish breast cancer patients

Por Allinen, M, Launonen, V, Laake, K, Jansen, L, Huusko, P, Kaariainen, H, Borresen-Dale, A, Winqvist, R
Publicado em 2002

Familial pericentric inversion inv(8)(p23q11).

Por Boyd, H, Kaste, J, Hovi, E, Ritanen-Mohammed, U M, Kääriäinen, H, de la Chapelle, A, Lehesjoki, A E
Publicado em 1994

Overlapping submicroscopic deletions in Xq28 in two unrelated boys with developmental disorders: identification of a gene near FRAXE.

Por Gedeon, A K, Meinänen, M, Adès, L C, Kääriäinen, H, Gécz, J, Baker, E, Sutherland, G R, Mulley, J C
Publicado em 1995

Direct contact in inviting high‐risk members of hereditary colon cancer families to genetic counselling and DNA testing

Por Aktan‐Collan, K, Haukkala, A, Pylvänäinen, K, Järvinen, H J, Aaltonen, L A, Peltomäki, P, Rantanen, E, Kääriäinen, H, Mecklin, J‐P
Publicado em 2007

Reply: Increased risk of breast cancer among female relatives of patients with Ataxia-Telangiectasia: a causal relationship?

Por Olsen, J H, Hahnemann, J M D, Børresen-Dale, A-L, Tretli, S, Kleinerman, R, Sankila, R, Hammarström, L, Robsahm, T E, Kääriäinen, H, Bregård, A, Brøndum-Nielsen, K, Yuen, J, Tucker, M
Publicado em 2005

Breast and other cancers in 1445 blood relatives of 75 Nordic patients with ataxia telangiectasia

Por Olsen, J H, Hahnemann, J M D, Børresen-Dale, A-L, Tretli, S, Kleinerman, R, Sankila, R, Hammarström, L, Robsahm, T E, Kääriäinen, H, Bregård, A, Brøndum-Nielsen, K, Yuen, J, Tucker, M
Publicado em 2005

The molecular basis for Duchenne versus Becker muscular dystrophy: Correlation of severity with type of deletion

Por Koenig, M., Beggs, A. H., Moyer, M., Scherpf, S., Heindrich, K., Bettecken, T., Meng, G., Müller, C. R., Lindlöf, M., Kaariainen, H., de la Chapelle, A., Kiuru, A., Savontaus, M.-L., Gilgenkrantz, H., Récan, D., Chelly, J., Kaplan, J.-C., Covone, A. E., Archidiacono, N., Romeo, G., Liechti-Gallati, S., Schneider, V., Braga, S., Moser, H., Darras, B. T., Murphy, P., Francke, U., Chen, J. D., Morgan, G., Denton, M., Greenberg, C. R., Wrogemann, K., Blonden, L. A. J., van Paassen, H. M. B., van Ommen, G. J. B., Kunkel, L. M.
Publicado em 1989