Literature DB >> 2332009

Birth distribution in cystic fibrosis and phenylketonuria.

G Machill1, J Gedschold, S Kropf.   

Abstract

The present study of 977 cystic fibrosis (CF) patients showed a bimodal birth distribution with peaks in April to July and October to January. After adjustment to the monthly variation of the birth rate of all liveborn children there was no significant deviation from the expected distribution. The 387 phenylketonuria (PKU) patients showed no seasonal birth variation.

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Year:  1990        PMID： 2332009     DOI： 10.1007/bf02009660

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN： 0340-6199            Impact factor:   3.183


  5 in total

1.  Cystic fibrosis in the Netherlands.

Authors:  L P Ten Kate
Journal:  Int J Epidemiol       Date:  1977-03       Impact factor: 7.196

2.  Seasonal variation in the birth of children with aneuploid chromosome abnormalities. Report from the Danish Cytogenetic Central Register.

Authors:  J Nielsen; G B Petersen; A J Therkelsen
Journal:  Humangenetik       Date:  1973

3.  Cystic fibrosis and the month of birth.

Authors:  T J David; G A Elstow; J H Baumer; C M Evans
Journal:  J Med Genet       Date:  1981-08       Impact factor: 6.318

4.  The seasonal variation of births of offspring from couples heterozygous for cystic fibrosis.

Authors:  C J Brackenridge
Journal:  Ann Hum Genet       Date:  1978-10       Impact factor: 1.670

5.  Bimodal month of birth distribution in cystic fibrosis.

Authors:  C J Brackenridge
Journal:  Am J Med Genet       Date:  1980
  5 in total
  1 in total

1.  Birth distribution in cystic fibrosis in Saguenay-Lac-St-Jean, Quebec, Canada.

Authors:  J Daigneault; G Aubin; F Simard; M De Braekeleer
Journal:  J Med Genet       Date:  1991-09       Impact factor: 6.318
  1 in total

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