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9p Trisomy; A New Case Due to Maternal t(9;18) Translocation

Published online by Cambridge University Press:  01 August 2014

A. Preto ,
E. Lenzini ,
P. Drigo ,
G. Fasoli  and
A. De Pascale
A. Preto*
Affiliation:
Laboratory of Cytogenetics, Department of Pediatrics, University of Padova, Italy
E. Lenzini
Affiliation:
Laboratory of Cytogenetics, Department of Pediatrics, University of Padova, Italy
P. Drigo
Affiliation:
Department of Pediatrics, University of Padova, Italy
G. Fasoli
Affiliation:
Heart Surgery Center, University of Padova, Italy
A. De Pascale
Affiliation:
Pediatric Division, Camposanpiero Hospital, Padova, Italy
*
Servizio di Citogenetica, Clinica Pediatrica, Università di Padova, Italy

Abstract

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A case of a patient carrying a 9p trisomy due to a maternal t(9;18) (p 13;p11) translocation is reported. In addition to the principal findings which characterize the 9p trisomy syndrome, this case presents some dysmorphic features due to the partial deletion of chromosome 18.

Type
Brief Report
Information
Acta geneticae medicae et gemellologiae: twin research , Volume 26 , Issue 3-4 , October 1977 , pp. 283 - 286
Copyright
Copyright © The International Society for Twin Studies 1977

References

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