Literature DB >> 7449182

Prenatal diagnosis of a de novo reciprocal translocation 46,XX,t(1;18) (p22;q23).

L Bovicelli, L F Orsini, N Rizzo, V Montacuti, M Bacchetta.   

Abstract

Mesh：

Year:  1980        PMID： 7449182     DOI： 10.1111/j.1399-0004.1980.tb01789.x

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


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  2 in total

1.  Reciprocal translocation t(1;18)(p32;q21) in a patient with some phenotypical anomalies.

Authors:  R Gil; C López-Ginés; M Gregori-Romero; M D Sánchez; A Pellin
Journal:  Hum Genet       Date:  1987-12       Impact factor: 4.132

2.  Acrocephalopolysyndactyly, pentalogy of Fallot, and hypoacusis in a patient with a de novo reciprocal translocation involving the short arm of chromosome 1 and the long arm of chromosome 18: 46,XX,t(1;18)(p31;q11).

Authors:  J Ward; E Vieto; D Lee; G Arosemena
Journal:  J Med Genet       Date:  1993-05       Impact factor: 6.318
  2 in total

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