Literature DB >> 8275560

Parental origin of the supernumerary chromosome in trisomy 18.

X Ya-gang1, W P Robinson, R Spiegel, F Binkert, U Ruefenacht, A A Schinzel.   

Abstract

The parental origin of an extra chromosome in Edwards syndrome has been investigated in 23 families by the combination of the VNTR probe pERT25, two microsatellite polymorphisms for D18S34 and D18S40, and several two-allele polymorphisms. Of the 23 cases, 22 were informative, with 17 (77%) being maternal and 5 (23%) paternal in origin. These results support the previous investigations, suggesting that trisomy 18 is predominantly of maternal origin, although a higher rate of paternally derived cases was observed than previously reported. A significant increase in maternal age was found to be associated with meiotic nondisjunction. Parental age was increased in both the maternally and paternally derived cases, but the size of the latter class was small and did not reach statistical significance.

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Year:  1993        PMID: 8275560     DOI: 10.1111/j.1399-0004.1993.tb03847.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  6 in total

1.  Incidence of chromosome 18 disomy in human sperm nuclei as detected by nonisotopic in situ hybridization.

Authors:  M Guttenbach; R Schakowski; M Schmid
Journal:  Hum Genet       Date:  1994-04       Impact factor: 4.132

2.  Trisomy 18: studies of the parent and cell division of origin and the effect of aberrant recombination on nondisjunction.

Authors:  J M Fisher; J F Harvey; N E Morton; P A Jacobs
Journal:  Am J Hum Genet       Date:  1995-03       Impact factor: 11.025

3.  Molecular studies of chromosomal mosaicism: relative frequency of chromosome gain or loss and possible role of cell selection.

Authors:  W P Robinson; F Binkert; F Bernasconi; I Lorda-Sanchez; E A Werder; A A Schinzel
Journal:  Am J Hum Genet       Date:  1995-02       Impact factor: 11.025

4.  Trisomy of human chromosome 18: molecular studies on parental origin and cell stage of nondisjunction.

Authors:  T Eggermann; M M Nöthen; B Eiben; D Hofmann; K Hinkel; R Fimmers; G Schwanitz
Journal:  Hum Genet       Date:  1996-02       Impact factor: 4.132

5.  The use of foetal ovarian stromal cell culture for cytogenetic diagnosis. Stromal ovarian culture cytogenetic diagnosis.

Authors:  I Roig; I Vanrell; A Ortega; Ll Cabero; J Egozcue; M Garcia
Journal:  Cytotechnology       Date:  2003-01       Impact factor: 2.058

6.  Single-Cell Transcriptomics of Cultured Amniotic Fluid Cells Reveals Complex Gene Expression Alterations in Human Fetuses With Trisomy 18.

Authors:  Jing Wang; Zixi Chen; Fei He; Trevor Lee; Wenjie Cai; Wanhua Chen; Nan Miao; Zhiwei Zeng; Ghulam Hussain; Qingwei Yang; Qiwei Guo; Tao Sun
Journal:  Front Cell Dev Biol       Date:  2022-03-22
  6 in total

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