Literature DB >> 7315808

Karyotype-phenotype correlation in partial trisomy 13. Report of a case due to maternal translocation.

E Bonioli, M Crisalli, R Monteverde, M G Vianello.   

Abstract

A partial trisomy 13q, originating from a maternal translocation, 46,XX,t(3;13) (p26;q22), occurred in a 3-month-old infant, affected by multiple congenital anomalies. A review of the previously reported cases of partial trisomy for the distal segment of the long arm of chromosome 13 is conclusive for the existence of a distinct clinical entity; however, it is difficult to assign particular malformations to specific chromosome bands.

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Year:  1981        PMID: 7315808     DOI: 10.1001/archpedi.1981.02130360023009

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  4 in total

1.  Phenotype-karyotype correlation in patients trisomic for various segments of chromosome 13.

Authors:  S A Tharapel; R C Lewandowski; A T Tharapel; R S Wilroy
Journal:  J Med Genet       Date:  1986-08       Impact factor: 6.318

2.  Elucidation of the centromere involvement in an inversion (13) by fluorescent in situ hybridisation.

Authors:  P L Gordon; J D Dalton; P R Martens; A T Tharapel; R S Wilroy
Journal:  J Med Genet       Date:  1993-05       Impact factor: 6.318

3.  The phenotype in partial 13q trisomies, apropos of a familial (13;15)(q22;q26) translocation.

Authors:  F Rivas; H Rivera; M L Plascencia; B Ibarra; J M Cantú
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

4.  Familial inversion translocation (8;13) with partial trisomy 13 in several family members.

Authors:  B Pilgaard; E Jørgensen; V S Knudsen; E Mortensen; M Mikkelsen
Journal:  Eur J Pediatr       Date:  1983-04       Impact factor: 3.183

  4 in total

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