Literature DB >> 7129451

Incidence of chromosome abnormalities in newborn children. Comparison between incidences in 1969-1974 and 1980-1982 in the same area.

J Nielsen, M Wohlert, J Faaborg-Andersen, K B Hansen, L Hvidman, B Krag-Olsen, I Moulvad, P Videbech.   

Abstract

As part of an ongoing study of the influence of environmental factors on pregnancy, childbirth, and fetuses, comparisons have been made between incidences in 1969-1974 and in 1980-1982 of chromosome aberrations in liveborn children in the same area of Denmark. The incidence of chromosome aberrations in the first period was 2.6 per 1000, compared with 41. per 1000 during the latter period. However, the difference was mainly due to an increase in inversions, and this in turn was due to a difference in chromosome staining methods between the two periods. It is concluded that the Danish study and similar studies in the United States, Canada, and Scotland indicate that early detection of chromosome aberrations by chromosome examination at birth is indicated in order to be able to inform and counsel parents of children with chromosome aberrations. Chromosome examination at birth is also of importance in the diagnosis of structural inheritable chromosome aberrations and consequent family investigation and genetic counseling.

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Year:  1982        PMID: 7129451     DOI: 10.1007/bf00274195

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  9 in total

1.  A psychiatric-psychological study of XYY males found in a general male population.

Authors:  E Zeuthen; M Hansen; A L Christensen; J Nielsen
Journal:  Acta Psychiatr Scand       Date:  1975-01       Impact factor: 6.392

2.  Criminality in XYY and XXY men.

Authors:  H A Witkin; S A Mednick; F Schulsinger; E Bakkestrom; K O Christiansen; D R Goodenough; K Hirschhorn; C Lundsteen; D R Owen; J Philip; D B Rubin; M Stocking
Journal:  Science       Date:  1976-08-13       Impact factor: 47.728

3.  Follow-up until age 4 to 8 of 25 unselected children with sex chromosome abnormalities, compared with sibs and controls.

Authors:  J Nielsen; I Sillesen; A M Sørensen; K Sørensen
Journal:  Birth Defects Orig Artic Ser       Date:  1979

4.  Assignment of the major histocompatibility complex to chromosome No. 6 in a family with a pericentric inversion.

Authors:  L U Lamm; U Friedrich; C B Petersen; J Jorgensen; J Nielsen; A J Therkelsen; F Kissmeyer-Nielsen
Journal:  Hum Hered       Date:  1974       Impact factor: 0.444

Review 5.  Behavioral implications of the human XYY genotype.

Authors:  E B Hook
Journal:  Science       Date:  1973-01-12       Impact factor: 47.728

6.  Thirty-five males with double Y chromosome.

Authors:  J Nielsen; A L Christensen
Journal:  Psychol Med       Date:  1974-02       Impact factor: 7.723

7.  Klinefelter's syndrome and the XXY syndrome. A genetical, endocrinological and psychiatric-psychological study of thirty-three severely hypogonadal male patients and two patients with karyotype 47,XYY.

Authors:  J Nielsen
Journal:  Acta Psychiatr Scand Suppl       Date:  1969

8.  Letter: Rates of XYY genotype in penal and mental settings.

Authors:  E B HOOK
Journal:  Lancet       Date:  1975-01-11       Impact factor: 79.321

9.  Mental development of unselected children with sex chromosome abnormalities.

Authors:  J Nielsen; A M Sørensen; K Sørensen
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

  9 in total
  12 in total

1.  Chromosome abnormalities found among 34,910 newborn children: results from a 13-year incidence study in Arhus, Denmark.

Authors:  J Nielsen; M Wohlert
Journal:  Hum Genet       Date:  1991-05       Impact factor: 4.132

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

Authors:  P A Jacobs; C Browne; N Gregson; C Joyce; H White
Journal:  J Med Genet       Date:  1992-02       Impact factor: 6.318

3.  Pericentric inversion of chromosome 9 in infertile men.

Authors:  I Sasagawa; M Ishigooka; Y Kubota; M Tomaru; T Hashimoto; T Nakada
Journal:  Int Urol Nephrol       Date:  1998       Impact factor: 2.370

Review 4.  Risk calculations for hereditary effects of ionizing radiation in humans.

Authors:  F Vogel
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

Review 5.  Incidence of congenital heart disease: II. Prenatal incidence.

Authors:  J I Hoffman
Journal:  Pediatr Cardiol       Date:  1995 Jul-Aug       Impact factor: 1.655

6.  Segregation analysis in a man heterozygous for a pericentric inversion of chromosome 7 (p13;q36) by sperm chromosome studies.

Authors:  J Navarro; J Benet; M R Martorell; C Templado; J Egozcue
Journal:  Am J Hum Genet       Date:  1993-07       Impact factor: 11.025

7.  Bilateral retinoblastoma with de novo constitutional balanced translocation t(2;9)(q11;p11).

Authors:  P Balestrazzi; M G Mattei; M A Baeteman; J F Mattei; F Giraud
Journal:  Eur J Pediatr       Date:  1984-02       Impact factor: 3.183

8.  A genotoxic study of metal workers exposed to trichloroethylene. Sperm parameters and chromosome aberrations in lymphocytes.

Authors:  K Rasmussen; S Sabroe; M Wohlert; H J Ingerslev; B Kappel; J Nielsen
Journal:  Int Arch Occup Environ Health       Date:  1988       Impact factor: 3.015

9.  Franceschetti syndrome in a child with a de novo balanced translocation (5;13)(q11;p11) and significant decrease of hexosaminidase B.

Authors:  P Balestrazzi; M A Baeteman; M G Mattei; J F Mattei
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

10.  Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.

Authors:  Bradford Coffee; Krayton Keith; Igor Albizua; Tamika Malone; Julie Mowrey; Stephanie L Sherman; Stephen T Warren
Journal:  Am J Hum Genet       Date:  2009-10       Impact factor: 11.025

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