Literature DB >> 2777262

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

M Gregori-Romero1, C López-Ginés, R Gil, A Pellín.   

Abstract

The authors report a case of 1;17 translocation and request contact with colleagues who have observed similar cases.

Entities:  

Mesh：

Year:  1989        PMID： 2777262     DOI： 10.1007/BF00286721

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  3 in total

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

Authors:  A de la Chapelle; R C Miller; A E Greene; L L Coriell
Journal:  Cytogenet Cell Genet       Date:  1975

2.  Familial Translocation t(1;17).

Authors:  Peter Steinbach
Journal:  Hum Genet       Date:  1981-10       Impact factor: 4.132

3.  A rapid banding technique for human chromosomes.

Authors:  M Seabright
Journal:  Lancet       Date:  1971-10-30       Impact factor: 79.321
  3 in total

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