Estimates of the frequency of chromosome abnormalities detectable in unselected newborns using moderate levels of banding.

Author:

Jacobs P A,Browne C,Gregson N,Joyce C,White H

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference10 articles.

1. The frequency of chromosome abnormalities detected in consecutive newbom studies differences between studies - results by sex and by severity of phenotypic involvement;Hook, E.B.; Hamerton, J.L.,1975

2. Chromosome analysis on 930 consecutive newborn children using_quinacrine fluorescent banding technique;Lin, C.C.; Gedeon, M.M.; Griffith, P.;Hum Genet,1976

3. A G-band study of chromosomes in liveborn infants;Buckton, K.E.; O'Riordan, M.L.; Ratcliffe, S.; Slight, J.; Mitchell, M.; McBeath, S.;Ann Hum Genet,1980

4. Incidence of chromosome abnormalities in newborn children. Comparison between incidences in 1969-1974 and 1980-1982 in the same area;Nielsen, J.; Wohlert, M.; Faaborg-Andersen, J.;Hum Genet,1982

5. Cytogenetic screening of a new-born population;Hansteen, I.-L.; Varslot, K.; Steen-Johnsen, J.; Langard, S.;Clin Genet,1982

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