Literature DB >> 5316133

Structural abnormalities of chromosome 18. II. Two familial translocations, B-18 and 16-18, ascertained through unbalanced forms.

B Eriksson, M Fraccaro, M Hultén, J Lindsten, C Thorén, L Tiepolo.   

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Year:  1971        PMID： 5316133

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


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  14 in total

Review 1.  Trisomy 16q23----qter arising from a maternal t(13;16)(p12;q23): case report and evidence of the reciprocal balanced maternal rearrangement by the Ag-NOR technique.

Authors:  J B Savary; F Vasseur; S Manouvrier; A Daudignon; O Lemaire; M Thieuleux; M Poher; P Lequien; M M Deminatti
Journal:  Hum Genet       Date:  1991-11       Impact factor: 4.132

2.  Partial trisomy 16q resulting from maternal translocation.

Authors:  P Balestrazzi; G Giovannelli; L Landucci Rubini; B Dallapiccola
Journal:  Hum Genet       Date:  1979-06-19       Impact factor: 4.132

Review 3.  [Ring chromosome 18. 18p-/18q- -deletion-syndrome].

Authors:  J Kunze; E Stephan; M Tolksdorf
Journal:  Humangenetik       Date:  1972

4.  Trisomy-18 syndrome caused by translocation or isochromosome formation. A case report with bibliography.

Authors:  H Müller; E M Bühler; E Signer; F Egli; G R Stalder
Journal:  J Med Genet       Date:  1972-12       Impact factor: 6.318

5.  Omphalocele and partial trisomy 1q syndrome.

Authors:  H Chen; J J Gershanik; J B Mailhes; I D Sanusi
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

6.  Duplication of 16q22-->qter confirmed by fluorescence in situ hybridisation and molecular analysis.

Authors:  R S Houlston; R M Renshaw; R S James; R Ironton; I K Temple
Journal:  J Med Genet       Date:  1994-11       Impact factor: 6.318

7.  Inclusion of satellites in an 18/21 translocation chromosome shown by ammonical-silver staining (sat-banding) in case of partial trisomy 18.

Authors:  R L Neu; C C Ortega; G A Barg; W Pinto; L I Gardner; W M Howell; T E Denton
Journal:  J Med Genet       Date:  1976-12       Impact factor: 6.318

8.  Trisomy 16q13----qter in a infant from a t(11;16)(q25;q13) translocation-carrier father.

Authors:  K Hatanaka; M Ozaki; M Suzuki; R Murata; H Fujita
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

9.  Trisomy 16q21 = to qter.

Authors:  A Garau; G Crisponi; D Peretti; R Vanni; O Zuffardi
Journal:  Hum Genet       Date:  1980-02       Impact factor: 4.132

10.  Trisomy 16p in a liveborn infant and a review of partial and full trisomy 16.

Authors:  S H Roberts; D P Duckett
Journal:  J Med Genet       Date:  1978-10       Impact factor: 6.318
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