Literature DB >> 48495

The value of fluorescence markers in the distinction between maternal and fetal chromosomes.

M Hauge, H Poulsen, A Halberg, M Mikkelsen.   

Abstract

Selected fluorescence markers of chromosomes were studied in 50 paired samples of cells obtained by culture of amniocentesis material and by culture of leukocytes from pregnant women. Comparative analyses showed that this method is of great value in disclosing admixture of maternal cells to material obtained by amniocentesis, as a minimum of 2 fluorescence marker differences between mother and fetus was found in the present material. The distribution of markers in mother/fetus pairs is in agreement with the assumption of genetic determination. Variation was observed between populations with respect to the frequency of the markers studied.

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Year:  1975        PMID： 48495     DOI： 10.1007/bf00281452

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


  2 in total

1.  Chromosome analysis of fetuses in risk pregnancies.

Authors:  J Philip; J Bang; N Hahnemann; M Mikkelsen; E Niebuhr; H Rebbe; J Weber
Journal:  Acta Obstet Gynecol Scand Suppl       Date:  1974

2.  Differential binding of alkylating fluorochromes in human chromosomes.

Authors:  T Caspersson; L Zech; C Johansson
Journal:  Exp Cell Res       Date:  1970-06       Impact factor: 3.905
  2 in total
  12 in total

1.  "Jumping" satellites in three generations: a warning for paternity tests and prenatal diagnosis.

Authors:  G Gimelli; E Porro; F Santi; S Scappaticci; O Zuffardi
Journal:  Hum Genet       Date:  1976-12-15       Impact factor: 4.132

2.  An abortus with a normal/trisomy 16 mosaicism: instability of trisomic cells in vitro.

Authors:  T Ikeuchi; M Sasaki
Journal:  Humangenetik       Date:  1975-11-06

3.  Maternal and paternal origin of extra chromosome in trisomy 21.

Authors:  M Mikkelsen; A Hallberg; H Poulsen
Journal:  Hum Genet       Date:  1976-04-15       Impact factor: 4.132

4.  Pitfalls in the use of chromosome variants for paternity dispute cases.

Authors:  Y Nakagome; T Kitagawa; K Iinuma; E Matsunaga; T Shinoda
Journal:  Hum Genet       Date:  1977-07-26       Impact factor: 4.132

5.  Chromosome polymorphism and twin zygosity.

Authors:  D L Van Dyke; C G Palmer; W E Nance; P L Yu
Journal:  Am J Hum Genet       Date:  1977-09       Impact factor: 11.025

6.  A photometric method for quantifying the polymorphisms in human acrocentric chromosomes.

Authors:  W Schnedl; U Roscher; R Czaker
Journal:  Hum Genet       Date:  1977-02-11       Impact factor: 4.132

7.  Prenatal diagnosis: techniques used to help in ruling out maternal cell contamination.

Authors:  D C Peakman; M F Moreton; A Robinson
Journal:  J Med Genet       Date:  1977-02       Impact factor: 6.318

8.  Use of genetic markers to certify fetal origin of cultured amniotic fluid cells.

Authors:  S H Chen; L E Karp; C R Scott; W Chen
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

9.  LBA technique in the detection of chromosome variants. I. Chromosomes with known sites of Q variants.

Authors:  S Oka; Y Nakagome; E Matsunaga; M Arima
Journal:  Hum Genet       Date:  1977-11-02       Impact factor: 4.132

Review 10.  Pericentric inversions. Problems and significance for clinical genetics.

Authors:  P Kaiser
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132
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