Literature DB >> 4584134

Hereditary diseases in Finland; rare flora in rare soul.

R Norio, H R Nevanlinna, J Perheentupa.   

Abstract

Entities:  

Mesh：

Year:  1973        PMID： 4584134

Source DB:  PubMed          Journal:  Ann Clin Res        ISSN： 0003-4762


× No keyword cloud information.
  65 in total

Review 1.  Finnish Disease Heritage I: characteristics, causes, background.

Authors:  Reijo Norio
Journal:  Hum Genet       Date:  2003-03-08       Impact factor: 4.132

Review 2.  The Finnish Disease Heritage III: the individual diseases.

Authors:  Reijo Norio
Journal:  Hum Genet       Date:  2003-03-08       Impact factor: 4.132

3.  Cartilage-hair hypoplasia in Finland: epidemiological and genetic aspects of 107 patients.

Authors:  O Mäkitie
Journal:  J Med Genet       Date:  1992-09       Impact factor: 6.318

4.  [Demographic reproduction and genetic transmission in the north-east of the province of Quebec (18th-20th centuries)].

Authors:  G Bouchard; C Laberge; C R Scriver
Journal:  Eur J Popul       Date:  1988-09

5.  Infantile cystinosis in France: genetics, incidence, geographic distribution.

Authors:  E Bois; J Feingold; P Frenay; M L Briard
Journal:  J Med Genet       Date:  1976-12       Impact factor: 6.318

6.  Linkage analysis of schizophrenia controlling for population substructure.

Authors:  Tiina Paunio; Ritva Arajärvi; Joseph D Terwilliger; Tero Hiekkalinna; Perttu Haimi; Timo Partonen; Jouko Lönnqvist; Leena Peltonen; Teppo Varilo
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2009-09-05       Impact factor: 3.568

7.  Genetic markers and population history: Finland revisited.

Authors:  Jukka U Palo; Ismo Ulmanen; Matti Lukka; Pekka Ellonen; Antti Sajantila
Journal:  Eur J Hum Genet       Date:  2009-04-15       Impact factor: 4.246

8.  Congenital chloride diarrhoea. Clinical analysis of 21 Finnish patients.

Authors:  C Holmberg; J Perheentupa; K Launiala; N Hallman
Journal:  Arch Dis Child       Date:  1977-04       Impact factor: 3.791

9.  Assignment of the locus for a new lethal neonatal metabolic syndrome to 2q33-37.

Authors:  I Visapää; V Fellman; T Varilo; A Palotie; K O Raivio; L Peltonen
Journal:  Am J Hum Genet       Date:  1998-11       Impact factor: 11.025

10.  Diagnostic criteria and genetics of the PEHO syndrome.

Authors:  M Somer
Journal:  J Med Genet       Date:  1993-11       Impact factor: 6.318
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.