Herpetiform keratitis and palmoplantar hyperkeratosis: warning signs for Richner-Hanhart syndrome (2017)
- Authors:
- USP affiliated author: KIM, CHONG AE - FM
- School: FM
- DOI: 10.1007%2Fs10545-016-9996-z
- Subjects: MUTAÇÃO GENÉTICA; DOENÇAS GENÉTICAS; BRASIL
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Journal of Inherited Metabolic Disease
- ISSN: 0141-8955
- Volume/Número/Paginação/Ano: v. 40, n. , p. 461-462, 2017
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
SOARES, Diogo C. et al. Herpetiform keratitis and palmoplantar hyperkeratosis: warning signs for Richner-Hanhart syndrome. Journal of Inherited Metabolic Disease, v. 40, n. , p. 461-462, 2017Tradução . . Disponível em: https://link.springer.com/content/pdf/10.1007%2Fs10545-016-9996-z.pdf. Acesso em: 01 jul. 2022. -
APA
Soares, D. C., Stroparo, M. N., Lian, Y. C., Takakura, C. Y., Wolf, S., Betz, R., & Kim, C. A. (2017). Herpetiform keratitis and palmoplantar hyperkeratosis: warning signs for Richner-Hanhart syndrome. Journal of Inherited Metabolic Disease, 40( ), 461-462. doi:10.1007%2Fs10545-016-9996-z -
NLM
Soares DC, Stroparo MN, Lian YC, Takakura CY, Wolf S, Betz R, Kim CA. Herpetiform keratitis and palmoplantar hyperkeratosis: warning signs for Richner-Hanhart syndrome [Internet]. Journal of Inherited Metabolic Disease. 2017 ; 40( ): 461-462.[citado 2022 jul. 01 ] Available from: https://link.springer.com/content/pdf/10.1007%2Fs10545-016-9996-z.pdf -
Vancouver
Soares DC, Stroparo MN, Lian YC, Takakura CY, Wolf S, Betz R, Kim CA. Herpetiform keratitis and palmoplantar hyperkeratosis: warning signs for Richner-Hanhart syndrome [Internet]. Journal of Inherited Metabolic Disease. 2017 ; 40( ): 461-462.[citado 2022 jul. 01 ] Available from: https://link.springer.com/content/pdf/10.1007%2Fs10545-016-9996-z.pdf - Clinical, cytogenetic, and molecular characterization of six patients with ring chromosomes 22, including one with concomitant 22q11.2 deletion
- Remote spinal cord injury in mucopolysaccharidosis type IVA after cervical decompression
- Cognitive and behavioral profile of Williams Syndrome toddlers
- Multimodal image analysis of the retina in Hunter syndrome (mucopolysaccharidosis type II): Case report
- Abordagem prática do paciente com malformação congênita
- Natural history of 39 patients with Achondroplasia
- NK and B cell deficiency in a MPS type II family with novel mutation in the IDS gene
- Contribuicao para o estudo da osteogenese imperfeita: aspectos genetico-clinicos de 25 casos
- Estudo genetico e clinico das amiotrofias espinhais progressivas
- Principais Síndromes de Origem Genética
Informações sobre o DOI: 10.1007%2Fs10545-016-9996-z (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
