Literature DB >> 5314290

A family with a presumptive C-F translocation in five generations.

A J Therkelsen, T Klinge, K Henningsen, M Mikkelsen, G Schmidt.   

Abstract

Mesh：

Year:  1971        PMID： 5314290

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


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  6 in total

1.  Partial trisomy 6p.

Authors:  A Bernheim; R Berger; G Vaugier; J C Thieffry; Y Matet
Journal:  Hum Genet       Date:  1979-04-17       Impact factor: 4.132

2.  Partial trisomy 6p due to familial translocation t(6;20)(p21;p13). A new syndrome?

Authors:  M H Breuning; J B Bijlsma; H F de France
Journal:  Hum Genet       Date:  1977-08-31       Impact factor: 4.132

3.  Partial trisomy 6p and partial trisomy 22 resulting from 3:1 meiotic disjunction of maternal (6p;22q) translocation.

Authors:  P R Scarbrough; A J Carroll; S C Finley; K Hamerick
Journal:  J Med Genet       Date:  1986-04       Impact factor: 6.318

4.  Inversion duplication of chromosome 6 with trisomic codominant expression of HLA antigens.

Authors:  G Pearson; J D Mann; J Bensen; R W Bull
Journal:  Am J Hum Genet       Date:  1979-01       Impact factor: 11.025

5.  Duplication 6p and deletion 9p.

Authors:  C Lytle; J Wade; A Farrier; F Flohrschutz; B Hecht; J Allanson
Journal:  J Med Genet       Date:  1989-01       Impact factor: 6.318

6.  Trisomy 6p22 leads to 6pter due to familial t(6;13)(p22;q34 or 33) translocation.

Authors:  G Rosi; G Venti; G Migliorini Brushelli; E Donti; V Bocchini; R Armellini
Journal:  Hum Genet       Date:  1979-09-02       Impact factor: 4.132
  6 in total

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