Literature DB >> 5588739

Familial 2/3 translocation.

W H Boon.   

Abstract

Mesh：

Year:  1967        PMID： 5588739

Source DB:  PubMed          Journal:  J Singapore Paediatr Soc        ISSN： 0037-5683


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  3 in total

1.  [Familial 2-C translocation: 46,XYt(2p-;Cp+) and 46,XXCp+].

Authors:  K Bender; H Reinwein; L Z Gorman; U Wolf
Journal:  Humangenetik       Date:  1969-10

2.  New chromosomal dysmorphic syndromes. 3. Partial trisomy 3q.

Authors:  S Stengel-Rutkowski; J D Murken; V Pilar; B Dutrillaux; A Rodewald; R Goebel; R Bassermann
Journal:  Eur J Pediatr       Date:  1979-02-08       Impact factor: 3.183

3.  Chromosome 3 duplication q21 leads to qter deletion p25 leads to pter syndrome in children of carriers of a pericentric inversion inv(3) (p25q21).

Authors:  P W Allderdice; N Browne; D P Murphy
Journal:  Am J Hum Genet       Date:  1975-11       Impact factor: 11.025
  3 in total

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