Literature DB >> 761416

Trisomy 20q due to maternal t(16;20) translocation. First case.

I H Pawlowitzki, H Gröbe, W Holzgreve.   

Abstract

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Year:  1979        PMID： 761416     DOI： 10.1111/j.1399-0004.1979.tb01756.x

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


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  3 in total

1.  Segregation of a t(3;20) translocation through three generations resulting in unbalanced karyotypes in six persons.

Authors:  K B Nielsen; N Tommerup; B Jespersen; P Nygaard; L Kleif
Journal:  J Med Genet       Date:  1986-10       Impact factor: 6.318

2.  Trisomy 20pter = to q11 in a malformed boy from a t(13;20)(p11;q11) translocation-carrier mother.

Authors:  A Schinzel
Journal:  Hum Genet       Date:  1980-02       Impact factor: 4.132

3.  Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. I. Cases due to deletions involving chromosome band 16p13.3.

Authors:  A O Wilkie; V J Buckle; P C Harris; J Lamb; N J Barton; S T Reeders; R H Lindenbaum; R D Nicholls; M Barrow; N C Bethlenfalvay
Journal:  Am J Hum Genet       Date:  1990-06       Impact factor: 11.025
  3 in total

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