Hietala M - Search Results

1

Acceptance of genetic testing in a general population: age, education and gender differences.

Aro AR, Hakonen A, Hietala M, Lönnqvist J, Niemelä P, Peltonen L, Aula P. Aro AR, et al. Among authors: hietala m. Patient Educ Couns. 1997 Sep-Oct;32(1-2):41-9. doi: 10.1016/s0738-3991(97)00061-x. Patient Educ Couns. 1997. PMID: 9355571

2

Attitudes toward genetic testing among the general population and relatives of patients with a severe genetic disease: a survey from Finland.

Hietala M, Hakonen A, Aro AR, Niemelä P, Peltonen L, Aula P. Hietala M, et al. Am J Hum Genet. 1995 Jun;56(6):1493-500. Am J Hum Genet. 1995. PMID: 7762573 Free PMC article.

3

Attitudes towards genetic testing: analysis of contradictions.

Jallinoja P, Hakonen A, Aro AR, Niemelä P, Hietala M, Lönnqvist J, Peltonen L, Aula P. Jallinoja P, et al. Among authors: hietala m. Soc Sci Med. 1998 May;46(10):1367-74. doi: 10.1016/s0277-9536(98)00017-3. Soc Sci Med. 1998. PMID: 9665567

4

Identification of a novel mutation causing aspartylglucosaminuria reveals a mutation hotspot region in the aspartylglucosaminidase gene.

Isoniemi A, Hietala M, Aula P, Jalanko A, Peltonen L. Isoniemi A, et al. Among authors: hietala m. Hum Mutat. 1995;5(4):318-26. doi: 10.1002/humu.1380050408. Hum Mutat. 1995. PMID: 7627186

5

Prospects of carrier screening of aspartylglucosaminuria in Finland.

Hietala M, Grön K, Syvänen AC, Peltonen L, Aula P. Hietala M, et al. Eur J Hum Genet. 1993;1(4):296-300. doi: 10.1159/000472427. Eur J Hum Genet. 1993. PMID: 8081942

6

[Attitudes toward genetic testing in Finland].

Aula P, Hietala M, Niemelä P, Aro AR, Hakonen A, Peltonen L. Aula P, et al. Among authors: hietala m. Duodecim. 1996;112(2):95-102. Duodecim. 1996. PMID: 10590612 Finnish. No abstract available.

7

DNA-based carrier screening in primary healthcare: screening for aspartylglucosaminuria mutations in maternity health offices.

Hietala M, Aula P, Syvänen AC, Isoniemi A, Peltonen L, Palotie A. Hietala M, et al. Clin Chem. 1996 Sep;42(9):1398-404. Clin Chem. 1996. PMID: 8787695

8

A retrospective study of long-term psychosocial consequences and satisfaction after carrier testing in childhood in an autosomal recessive disease: aspartylglucosaminuria.

Järvinen O, Hietala M, Aalto AM, Arvio M, Uutela A, Aula P, Kääriäinen H. Järvinen O, et al. Among authors: hietala m. Clin Genet. 2000 Dec;58(6):447-54. doi: 10.1034/j.1399-0004.2000.580604.x. Clin Genet. 2000. PMID: 11149613

9

Origin of Finnish mutations causing aspartylglucosaminuria.

Valkonen S, Hietala M, Savontaus ML, Aula P. Valkonen S, et al. Among authors: hietala m. Hereditas. 1999;131(3):191-5. doi: 10.1111/j.1601-5223.1999.t01-1-00191.x. Hereditas. 1999. PMID: 10783529 Free article.

10

MECP2 gene analysis in classical Rett syndrome and in patients with Rett-like features.

Auranen M, Vanhala R, Vosman M, Levander M, Varilo T, Hietala M, Riikonen R, Peltonen L, Järvelä I. Auranen M, et al. Among authors: hietala m. Neurology. 2001 Mar 13;56(5):611-7. doi: 10.1212/wnl.56.5.611. Neurology. 2001. PMID: 11245712

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

95 results

Search Page

Filters