Saethre–Chotzen phenotype with learning disability and hyper IgE phenotype in a patient due to complex chromosomal rearrangement involving chromosomes 3 and 7 (2012)
- Authors:
- USP affiliated authors: CEIDE, ROSELI MARIA ZECHI - HRAC ; NAKATA, NANCY MIZUE KOKITSU - HRAC ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB ; ALMEIDA, MARIA LEINE GUION DE - HRAC
- Unidades: HRAC; IB
- DOI: 10.1002/ajmg.a.35367
- Subjects: CROMOSSOMOS; GENÉTICA MÉDICA; GENES
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American Journal of Medical Genetics Part A
- ISSN: 1552-4833
- Volume/Número/Paginação/Ano: v. 158A, n. 7, p. 1680\20131685, Jul. 2012
- Este periódico é de assinatura
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: bronze
-
ABNT
ZECHI-CEIDE, Roseli Maria et al. Saethre–Chotzen phenotype with learning disability and hyper IgE phenotype in a patient due to complex chromosomal rearrangement involving chromosomes 3 and 7. American Journal of Medical Genetics Part A, v. 158A, n. 7, p. 1680\20131685, 2012Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.35367. Acesso em: 25 abr. 2024. -
APA
Zechi-Ceide, R. M., Rodrigues, M. G., Jehee, F. S., Nakata, N. M. K., Passos-Bueno, M. R., & Guion Almeida, M. L. (2012). Saethre–Chotzen phenotype with learning disability and hyper IgE phenotype in a patient due to complex chromosomal rearrangement involving chromosomes 3 and 7. American Journal of Medical Genetics Part A, 158A( 7), 1680\20131685. doi:10.1002/ajmg.a.35367 -
NLM
Zechi-Ceide RM, Rodrigues MG, Jehee FS, Nakata NMK, Passos-Bueno MR, Guion Almeida ML. Saethre–Chotzen phenotype with learning disability and hyper IgE phenotype in a patient due to complex chromosomal rearrangement involving chromosomes 3 and 7 [Internet]. American Journal of Medical Genetics Part A. 2012 ; 158A( 7): 1680\20131685.[citado 2024 abr. 25 ] Available from: https://doi.org/10.1002/ajmg.a.35367 -
Vancouver
Zechi-Ceide RM, Rodrigues MG, Jehee FS, Nakata NMK, Passos-Bueno MR, Guion Almeida ML. Saethre–Chotzen phenotype with learning disability and hyper IgE phenotype in a patient due to complex chromosomal rearrangement involving chromosomes 3 and 7 [Internet]. American Journal of Medical Genetics Part A. 2012 ; 158A( 7): 1680\20131685.[citado 2024 abr. 25 ] Available from: https://doi.org/10.1002/ajmg.a.35367 - Clinical evidence for a mandibular to maxillary transformation in auriculocondylar syndrome
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Informações sobre o DOI: 10.1002/ajmg.a.35367 (Fonte: oaDOI API)
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