Literature DB >> 4139001

An (X;1) translocation, balanced, 46 chromosomes. Repository identification no. GM-97.

H H Punnett, M L Kistermacher, A E Greene, L L Coriell.   

Abstract

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Mesh：

Year:  1974        PMID： 4139001     DOI： 10.1159/000130291

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


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  5 in total

1.  Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature.

Authors:  M J Pettenati; J L Haines; R R Higgins; R S Wappner; C G Palmer; D D Weaver
Journal:  Hum Genet       Date:  1986-10       Impact factor: 4.132

2.  X-autosome translocation with a breakpoint in Xq22 in a fertile woman and her 47,XXX infertile daughter.

Authors:  K Madan; P G Hompes; J Schoemaker; C E Ford
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

3.  Studies of malformation syndromes of man XXIX: the Wiedemann-Beckwith syndrome. Clinical, genetic and pathogenetic studies of 12 cases.

Authors:  A L Kosseff; J Herrmann; E F Gilbert; C Viseskul; M Lubinsky; J M Opitz
Journal:  Eur J Pediatr       Date:  1976-10-01       Impact factor: 3.183

4.  X-autosome translocations: cytogenetic characteristics and their consequences.

Authors:  M G Mattei; J F Mattei; S Ayme; F Giraud
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

Review 5.  Balanced structural changes involving the human X: effect on sexual phenotype.

Authors:  K Madan
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132
  5 in total

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