TRISOMIA 5P

Translated title of the contribution: Trisomy 5p

B. Dallapiccola, A. Calabro, A. Forabosco, G. Preto

Research output: Contribution to journalArticle

Abstract

Two patients are described with trisomy 5p, resulting from the segregation through 3 generations of a t(4:5) (q33 p14) translocation. In the same family, 2 subjects are affected by the 'cri du chat' syndrome. The complex of malformations observed in the 2 trisomic patients is closely comparable to that reported in the few, previously described cases. However, the nonspecific character of these malformations makes trisomy 5p not yet clinically definable as a syndrome.

Original languageItalian
Pages (from-to)63-73
Number of pages11
JournalActa Medica Auxologica
Volume8
Issue number1
Publication statusPublished - 1976

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Trisomy
Cri-du-Chat Syndrome

ASJC Scopus subject areas

  • Medicine(all)

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Dallapiccola, B., Calabro, A., Forabosco, A., & Preto, G. (1976). TRISOMIA 5P. Acta Medica Auxologica, 8(1), 63-73.

TRISOMIA 5P. / Dallapiccola, B.; Calabro, A.; Forabosco, A.; Preto, G.

In: Acta Medica Auxologica, Vol. 8, No. 1, 1976, p. 63-73.

Research output: Contribution to journalArticle

Dallapiccola, B, Calabro, A, Forabosco, A & Preto, G 1976, 'TRISOMIA 5P', Acta Medica Auxologica, vol. 8, no. 1, pp. 63-73.
Dallapiccola B, Calabro A, Forabosco A, Preto G. TRISOMIA 5P. Acta Medica Auxologica. 1976;8(1):63-73.
Dallapiccola, B. ; Calabro, A. ; Forabosco, A. ; Preto, G. / TRISOMIA 5P. In: Acta Medica Auxologica. 1976 ; Vol. 8, No. 1. pp. 63-73.
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