TRISOMIA 5P

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

TRISOMIA 5P

Translated title of the contribution: Trisomy 5p

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

Ospedale Pediatrico Bambino Gesu

Research output: Contribution to journal › Article › peer-review

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.

Translated title of the contribution	Trisomy 5p
Original language	Italian
Pages (from-to)	63-73
Number of pages	11
Journal	Acta Medica Auxologica
Volume	8
Issue number	1
Publication status	Published - 1976

ASJC Scopus subject areas

Medicine(all)

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title = "TRISOMIA 5P",

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.",

author = "B. Dallapiccola and A. Calabro and A. Forabosco and G. Preto",

year = "1976",

language = "Italian",

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AU - Dallapiccola, B.

AU - Calabro, A.

AU - Forabosco, A.

AU - Preto, G.

PY - 1976

Y1 - 1976

N2 - 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.

AB - 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.

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