Literature DB >> 2798350

Chromosome mosaicism of the placenta--a cause of developmental failure of the fetus?

E Schwinger1, E Seidl, F Klink, H Rehder.   

Abstract

Fourteen (2.5 per cent) of 568 chromosome preparations after CVS showed discrepancies between the placental and fetal karyotype, mainly due to placental mosaicism. The presence of a second cell line within the placenta was confirmed in all but one case, in which cytogenetic reinvestigations were carried out. Our clinical data indicate that severe developmental retardation in the newborn is not to be expected if only the placenta carries the chromosomally abnormal cell line.

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Year:  1989        PMID: 2798350     DOI: 10.1002/pd.1970090907

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  5 in total

1.  Distribution of mosaicism in human placentae.

Authors:  K G Henderson; T E Shaw; I J Barrett; A H Telenius; R D Wilson; D K Kalousek
Journal:  Hum Genet       Date:  1996-05       Impact factor: 4.132

Review 2.  Confined placental mosaicism.

Authors:  D K Kalousek; M Vekemans
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

3.  Detection of confined placental mosaicism in trisomy 18 conceptions using interphase cytogenetic analysis.

Authors:  K J Harrison; I J Barrett; B L Lomax; B D Kuchinka; D K Kalousek
Journal:  Hum Genet       Date:  1993-10       Impact factor: 4.132

4.  Uniparental disomy for chromosome 16 in humans.

Authors:  D K Kalousek; S Langlois; I Barrett; I Yam; D R Wilson; P N Howard-Peebles; M P Johnson; E Giorgiutti
Journal:  Am J Hum Genet       Date:  1993-01       Impact factor: 11.025

5.  Prenatal and postnatal prevalence of Turner's syndrome: a registry study.

Authors:  C H Gravholt; S Juul; R W Naeraa; J Hansen
Journal:  BMJ       Date:  1996-01-06
  5 in total

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