Literature DB >> 7069750

A malformed baby with two separate de novo translocations.

W E Chewings, T P Cocks, R J Gardner, J E Clarkson.   

Abstract

Mesh：

Year:  1982        PMID： 7069750      PMCID： PMC1048823          DOI： 10.1136/jmg.19.1.70

Source DB:  PubMed          Journal:  J Med Genet        ISSN： 0022-2593            Impact factor:   6.318


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  6 in total

1.  Prenatal diagnosis and postnatal follow-up of an abnormal child with two de novo apparently balanced translocations.

Authors:  C Stoll; E Flori; J Macler; R Renaud
Journal:  Hum Genet       Date:  1979-03-12       Impact factor: 4.132

2.  [46, XX, 1q-, 2q-, Dq+, 16q+ karyotype in a polymalformed child].

Authors:  J de Grouchy; F Lautmann
Journal:  Ann Genet       Date:  1968-06

3.  Double translocation t(7;12),t(2;6) heterozygosity in one family. A contribution to the trisomy 12p syndrome.

Authors:  J B Bijlsma; H F de France; L M Bleeker-Wagemakers; P F Dijkstra
Journal:  Hum Genet       Date:  1978-01-19       Impact factor: 4.132

4.  A woman carrier of two apparently unrelated reciprocal translocations: prenatal diagnosis of normal karyotype in the foetus.

Authors:  G Simoni; E Montali; F Rossella; L Dalprà; F Lo Curto
Journal:  Hum Genet       Date:  1979-01-25       Impact factor: 4.132

5.  Two reciprocal translocations associated with microcephaly and retardation.

Authors:  E F Bell; D Warburton
Journal:  J Med Genet       Date:  1977-04       Impact factor: 6.318

6.  Apparently balanced de novo translocations in patients with abnormal phenotypes: report of 6 cases.

Authors:  A T Tharapel; R L Summitt; R S Wilroy; P Martens
Journal:  Clin Genet       Date:  1977-04       Impact factor: 4.438
  6 in total

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