Literature DB >> 4253289

Secondary nondisjunction causing regular trisomy 21 in the offspring of a mosaic trisomy 21 mother.

E Krmpotic, M B Hardin.   

Abstract

Mesh：

Year:  1971        PMID： 4253289     DOI： 10.1016/0002-9378(71)90705-8

Source DB:  PubMed          Journal:  Am J Obstet Gynecol        ISSN： 0002-9378            Impact factor:   8.661


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  4 in total

1.  Turner phenotype: mosaic 45,X-47,XY, plus 18.

Authors:  A Schinzel; W Schmid; A Prader
Journal:  J Med Genet       Date:  1974-03       Impact factor: 6.318

2.  Paternal trisomy 21 mosaicism and Down's anomaly.

Authors:  K Méhes
Journal:  Humangenetik       Date:  1973

3.  Germ-line transmission of trisomy 21: Data from 80 families suggest an implication of grandmaternal age and a high frequency of female-specific trisomy rescue.

Authors:  Natalia V Kovaleva
Journal:  Mol Cytogenet       Date:  2010-03-18       Impact factor: 2.009

4.  Parental trisomy 21 mosaicism.

Authors:  D J Harris; M L Begleiter; J Chamberlin; L Hankins; R E Magenis
Journal:  Am J Hum Genet       Date:  1982-01       Impact factor: 11.025
  4 in total

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