Literature DB >> 3692481

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

R Gil1, C López-Ginés, M Gregori-Romero, M D Sánchez, A Pellin.   

Abstract

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Year:  1987        PMID： 3692481     DOI： 10.1007/bf00291431

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


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  3 in total

1.  Translocation heterozygosity and associated subfertility in man.

Authors:  A C Chandley; S Christie; J Fletcher; A Frackiewicz; P A Jacobs
Journal:  Cytogenetics       Date:  1972

2.  The use of proteolytic enzymes for the mapping of structural rearrangements in the chromosomes of man.

Authors:  M Seabright
Journal:  Chromosoma       Date:  1972       Impact factor: 4.316

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

Authors:  L Bovicelli; L F Orsini; N Rizzo; V Montacuti; M Bacchetta
Journal:  Clin Genet       Date:  1980-12       Impact factor: 4.438
  3 in total

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