Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jussi Kärnä"'
Publikováno v:
Clinical Genetics. 32:192-195
A linkage study was carried out in nine families with 24 males affected by X-linked recessive retinoschisis (RS), using three polymorphic DNA probes from the distal segment of Xp. Close linkage of the disease locus with markers DXS41 (probe p99-6) an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84aa05674b4ef6c45031ab2283b9d53c
https://doi.org/10.1111/j.1399-0004.1987.tb03353.x
https://doi.org/10.1111/j.1399-0004.1987.tb03353.x
Publikováno v:
Clinical Genetics. 29:471-472
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a52ebdf1c1d588255d27807bd2be5894
https://doi.org/10.1111/j.1399-0004.1986.tb00541.x
https://doi.org/10.1111/j.1399-0004.1986.tb00541.x
Publikováno v:
Acta ophthalmologica Scandinavica. 73(4)
The purpose of the paper is to describe results of combined use of argon laser photocoagulation and cryotherapy in the treatment of stage 3+ retinopathy of prematurity in a non-controlled clinical series of 6 premature children with a birth weight of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b94912b04f8c7a5189db518f50485fc3
https://pubmed.ncbi.nlm.nih.gov/8646579
https://pubmed.ncbi.nlm.nih.gov/8646579
Autor:
Jussi Kärnä, David C. Page, Jurg Ott, A. de la Chapelle, Thomas Lehner, E.-M. Sankila, H. Forsius, A. W. Eriksson
Publikováno v:
Human Genetics. 84:66-70
Multipoint linkage analysis of choroideremia (TCD) and seven X chromosomal restriction fragment length polymorphisms (RFLPs) was carried out in 18 Finnish TCD families. The data place TCD distal to PGK and DXS72, very close to DXYS1 and DXYS5 (Zmax =
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de60c59befe0a10c22574f00d96201db
https://doi.org/10.1007/bf00210674
https://doi.org/10.1007/bf00210674
Autor:
R. Miettinen, Ollila Oi, Larmi T, Takala J, Hannu I. Alanko, Ulf Krause, Jussi Kärnä, E. Jaanio
Publikováno v:
Acta ophthalmologica. Supplement. 184
Three separate investigations are reported, covering a total of 795 patients from different parts of Finland, two of them consisting of inmates of old people's homes in two towns (N = 205 and 262) and one a randomly selected population from a rural c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e403980218d5f97e02c91738dce39a6
https://pubmed.ncbi.nlm.nih.gov/2853908
https://pubmed.ncbi.nlm.nih.gov/2853908
Publikováno v:
Clinical genetics. 31(5)
Linkage studies using restriction fragment length polymorphisms were conducted in the X-linked disorder, choroideremia, designated TCD for Progressive Tapeto-Choroidal Dystrophy. Previously demonstrated close linkage with locus DXYS1 was confirmed (l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9001acb9254dd7857b28051effd27f82
https://pubmed.ncbi.nlm.nih.gov/2886237
https://pubmed.ncbi.nlm.nih.gov/2886237
Autor:
Heikki Aurekoski, R.R. Frants, Ahti Tarkkanen, Jussi Kärnä, Margareta Damsten, H. Forsius, Aldur W. Eriksson
Publikováno v:
Acta ophthalmologica. 61(4)
Ninety-two cases of granular corneal dystrophy, most of them belonging to 5 pedigrees are described. The age of manifestation in this Finnish type of granular dystrophy is first in the end of the second decade, and visual acuity is in mean normal thr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d632c1e7dbcb68e11a5695616473a3c6
https://pubmed.ncbi.nlm.nih.gov/6605646
https://pubmed.ncbi.nlm.nih.gov/6605646