Literature DB >> 2528151

Genetic risk factors in human trisomy 21.

M Mikkelsen1, H Poulsen, N Tommerup.   

Abstract

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Year:  1989        PMID： 2528151

Source DB:  PubMed          Journal:  Prog Clin Biol Res        ISSN： 0361-7742


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  3 in total

1.  No evidence for a paternal interchromosomal effect from analysis of the origin of nondisjunction in Down syndrome patients with concomitant familial chromosome rearrangements.

Authors:  A A Schinzel; P A Adelsberger; F Binkert; S Basaran; S E Antonarakis
Journal:  Am J Hum Genet       Date:  1992-02       Impact factor: 11.025

2.  Cytogenetic status of patients with congenital malformations or suspected chromosomal abnormalities in Turkey: a comprehensive cytogenetic survey of 11,420 patients.

Authors:  Osman Demirhan; Erdal Tunç
Journal:  Chromosoma       Date:  2022-10-11       Impact factor: 2.919

3.  Down syndrome due to de novo Robertsonian translocation t(14q;21q): DNA polymorphism analysis suggests that the origin of the extra 21q is maternal.

Authors:  M B Petersen; P A Adelsberger; A A Schinzel; F Binkert; G K Hinkel; S E Antonarakis
Journal:  Am J Hum Genet       Date:  1991-09       Impact factor: 11.025
  3 in total

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