3P DELETION SYNDROME AND CONGENITAL HEART DISEASE: CASE REPORT

Authors

  • Sílvia Pires Unidade de Citogenética, Centro Genética Médica Doutor Jacinto Magalhães, Centro Hospitalar do Porto
  • Natália Oliva-Teles Unidade de Citogenética, Centro Genética Médica Doutor Jacinto Magalhães, Centro Hospitalar do Porto; Unidade Multidisciplinar de Investigação Biomédica (UMIB)/ Instituto de Ciências Biomédicas Abel Salazar (ICBAS), Universidade do Porto
  • Manuela Mota Freitas Unidade de Citogenética, Centro Genética Médica Doutor Jacinto Magalhães, Centro Hospitalar do Porto; Unidade Multidisciplinar de Investigação Biomédica (UMIB)/ Instituto de Ciências Biomédicas Abel Salazar (ICBAS), Universidade do Porto
  • Dulce Oliveira Consulta de Neonatologia, Centro Materno-Infantil do Norte, Centro Hospitalar do Porto
  • Maria do Céu Rodrigues Centro de Diagnóstico Pré-Natal, Centro Materno-Infantil do Norte, Centro Hospitalar do Porto
  • Sílvia Álvares Serviço de Cardiologia Pediátrica, Centro Hospitalar do Porto
  • M Fonseca Silva Unidade de Citogenética, Centro Genética Médica Doutor Jacinto Magalhães, Centro Hospitalar do Porto

DOI:

https://doi.org/10.25753/BirthGrowthMJ.v25.i0.10535

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Published

2016-12-27

How to Cite

1.
Pires S, Oliva-Teles N, Freitas MM, Oliveira D, Rodrigues M do C, Álvares S, Silva MF. 3P DELETION SYNDROME AND CONGENITAL HEART DISEASE: CASE REPORT. REVNEC [Internet]. 2016Dec.27 [cited 2025May3];25:S24. Available from: https://revistas.rcaap.pt/nascercrescer/article/view/10535

Issue

Vol. 25 (2016): Supplement I: XLV Conferências de Genética Doutor Jacinto Magalhães

Section

Resumo dos posters

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