Literature DB >> 1132251

A (1;17) translocation, balanced, plus trisomy 21, 47 chromosomes. Repository identification No. GM-201.

A de la Chapelle, R C Miller, A E Greene, L L Coriell.   

Abstract

Mesh：

Year:  1975        PMID： 1132251     DOI： 10.1159/000130323

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN： 0301-0171


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  3 in total

1.  Familial balanced translocation 4p+/17q- as a suggested cause of primary trisomy-21 Down's syndrome.

Authors:  K Oikawa; M Trent; R Lebovitz
Journal:  Arch Dis Child       Date:  1977-11       Impact factor: 3.791

2.  Congenital hyperthyroidism with reciprocal translocation t(1;17)(q25;q21).

Authors:  M Gregori-Romero; C López-Ginés; R Gil; A Pellín
Journal:  Hum Genet       Date:  1989-09       Impact factor: 4.132

3.  Electrophoretic characterization and genetics of human biliverdin reductase (BLVR; EC 1.3.1.24); assignment of BLVR to the p14 leads to cen region of human chromosome 7 in mouse-human somatic cell hybrids.

Authors:  P Meera Khan; L M Wijnen; J T Wijnen; K H Grzeschik
Journal:  Biochem Genet       Date:  1983-02       Impact factor: 1.890
  3 in total

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