Mowat-Wilson syndrome: growth charts (2020)
- Authors:
- Autor USP: VALERA, ELVIS TERCI - FMRP
- Unidade: FMRP
- DOI: 10.1186/s13023-020-01418-4
- Subjects: MUTAÇÃO GENÉTICA; MALFORMAÇÕES; MORFOMETRIA
- Keywords: Mowat-Wilson syndrome; ZEB2; Growth charts; Weight; Length; Height; Head circumference; Body mass index; BMI
- Language: Inglês
- Imprenta:
- Source:
- Título: Orphanet Journal of Rare Diseases
- ISSN: 1750-1172
- Volume/Número/Paginação/Ano: v. 15, art. 151, p. 1-12, 2020
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
IVANOVSKI, Ivan et al. Mowat-Wilson syndrome: growth charts. Orphanet Journal of Rare Diseases, v. 15, p. 1-12, 2020Tradução . . Disponível em: https://doi.org/10.1186/s13023-020-01418-4. Acesso em: 12 fev. 2026. -
APA
Ivanovski, I., Djuric, O., Broccoli, S., Caraffi, S. G., Accorsi, P., Adam, M. P., et al. (2020). Mowat-Wilson syndrome: growth charts. Orphanet Journal of Rare Diseases, 15, 1-12. doi:10.1186/s13023-020-01418-4 -
NLM
Ivanovski I, Djuric O, Broccoli S, Caraffi SG, Accorsi P, Adam MP, Avela K, Badura-Stronka M, Bayat A, Clayton-Smith J, Cocco I, Valera ET. Mowat-Wilson syndrome: growth charts [Internet]. Orphanet Journal of Rare Diseases. 2020 ; 15 1-12.[citado 2026 fev. 12 ] Available from: https://doi.org/10.1186/s13023-020-01418-4 -
Vancouver
Ivanovski I, Djuric O, Broccoli S, Caraffi SG, Accorsi P, Adam MP, Avela K, Badura-Stronka M, Bayat A, Clayton-Smith J, Cocco I, Valera ET. Mowat-Wilson syndrome: growth charts [Internet]. Orphanet Journal of Rare Diseases. 2020 ; 15 1-12.[citado 2026 fev. 12 ] Available from: https://doi.org/10.1186/s13023-020-01418-4 - Estudo dos genes de resistência a drogas MDR-1, MRP e LRP em crianças portadoras de leucemia linfoblástica aguda através da reação em cadeia da polimerase da transcrição reversa (RT-PCR)
- Análise do perfil de expresão de genes relacionados à resistência múltipla a drogas em tumores do sistema nervoso central por PCR quantitativa
- Teratoma‐associated and so‐called pure Wilms tumour of the ovary represent two separate tumour types with distinct molecular features
- Isomorphic diffuse glioma is a morphologically and molecularly distinct tumour entity with recurrent gene fusions of MYBL1 or MYB and a benign disease course
- The multifaceted NF-kB: are there still prospects of its inhibition for clinical intervention in pediatric central nervous system tumors ?
- ADA2 deficiency (DADA2) associated with Evans syndrome and a severe ADA2 genotype. [carta]
- Beyond clinical trials: understanding neurotrophic tropomyosin receptor kinase inhibitor challenges and efficacy in real-world pediatric oncology
- The TK1 gene as a potential prognostic marker and its correlation with immune cell infiltrates in adrenocortical carcinoma: in silico analyses
- Short-term response to alemtuzumab in CD52-positive secondary histiocytic sarcoma in a child. [Carta]: Is it time to consider new targets?
- High frequency of WNT-activated medulloblastomas with CTNNB1 wild type suggests a higher proportion of hereditary cases in a Latin-Iberian population
Informações sobre o DOI: 10.1186/s13023-020-01418-4 (Fonte: oaDOI API)
Download do texto completo
| Tipo | Nome | Link | |
|---|---|---|---|
 |
003088296.pdf | Direct link |
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
