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Birth distribution in cystic fibrosis and phenylketonuria
Authors:G. Machill  J. Gedschold  S. Kropf
Affiliation:(1) Institut für Medizinische Genetik der Ernst-Moritz-Arndt-Universität, Fleischmannstrasse 42/44, DDR-2200 Greifswald, German Democratic Republic;(2) Abteilung Humangenetik, DDR-3090 Magdeburg, German Democratic Republic;(3) Abteilung für Biomathematik und Medizinische Informatik der Medizinischen Akademie, DDR-3090 Magdeburg, German Democratic Republic
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.
Keywords:Cystic fibrosis  Phenylketonuria  Birth distribution
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