Literature DB >> 5123495

The incidence of Pku in Finland.

J K Visakorpi, J Palo, O V Renkonen.   

Abstract

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Year:  1971        PMID： 5123495     DOI： 10.1111/j.1651-2227.1971.tb07007.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN： 0001-656X


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  5 in total

Review 1.  Disease gene mapping in isolated human populations: the example of Finland.

Authors:  A de la Chapelle
Journal:  J Med Genet       Date:  1993-10       Impact factor: 6.318

2.  Finnish national screening for hypothyroidism. Few false positives, early therapy.

Authors:  M Virtanen; J Perheentupa; J Mäenpää; L Pitkänen; J Pikkarainen
Journal:  Eur J Pediatr       Date:  1984-11       Impact factor: 3.183

3.  Successful adjustment to society by adults with phenylketonuria.

Authors:  R Koch; M Yusin; K Fishler
Journal:  J Inherit Metab Dis       Date:  1985       Impact factor: 4.982

4.  Birth prevalence of phenylalanine hydroxylase deficiency: a systematic literature review and meta-analysis.

Authors:  Pamela K Foreman; Andrea V Margulis; Kimberly Alexander; Renee Shediac; Brian Calingaert; Abenah Harding; Manel Pladevall-Vila; Sarah Landis
Journal:  Orphanet J Rare Dis       Date:  2021-06-03       Impact factor: 4.123

5.  Genetics in an isolated population like Finland: a different basis for genomic medicine?

Authors:  Helena Kääriäinen; Juha Muilu; Markus Perola; Kati Kristiansson
Journal:  J Community Genet       Date:  2017-07-20
  5 in total

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