Non-immune hydrops fetalis with long bones fragility: a new subtype of osteogenesis imperfecta type II or a new form of skeletal dysplasia ? (2017)
- Authors:
- USP affiliated authors: SILVA JUNIOR, WILSON ARAÚJO DA - FMRP ; MOLFETTA, GREICE ANDREOTTI DE - FMRP
- School: FMRP
- Subjects: OSTEOGÊNESE IMPERFEITA; GENÉTICA MÉDICA
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: Abstracts
- Conference title: Annual Meeting of the American Society of Human Genetics
-
ABNT
MOLFETTA, Greice Andreotti de; PIRAM, A.; MACHRY, A. J.; et al. Non-immune hydrops fetalis with long bones fragility: a new subtype of osteogenesis imperfecta type II or a new form of skeletal dysplasia ? Anais.. Orlando: ASHG, 2017. -
APA
Molfetta, G. A. de, Piram, A., Machry, A. J., Anjos, T. O., Marques, A. A., & Silva Júnior, W. A. da. (2017). Non-immune hydrops fetalis with long bones fragility: a new subtype of osteogenesis imperfecta type II or a new form of skeletal dysplasia ? In Abstracts. Orlando: ASHG. -
NLM
Molfetta GA de, Piram A, Machry AJ, Anjos TO, Marques AA, Silva Júnior WA da. Non-immune hydrops fetalis with long bones fragility: a new subtype of osteogenesis imperfecta type II or a new form of skeletal dysplasia ? Abstracts. 2017 ; -
Vancouver
Molfetta GA de, Piram A, Machry AJ, Anjos TO, Marques AA, Silva Júnior WA da. Non-immune hydrops fetalis with long bones fragility: a new subtype of osteogenesis imperfecta type II or a new form of skeletal dysplasia ? Abstracts. 2017 ; - Identification of genes silenced by methylation on head and neck tumor cell lineages
- Novas mutações identificadas nos genes COL1A1 E COL1A2 em pacientes com osteogênese imperfeita
- Qualitative analysis of lncRNAs in the melanoma progression
- Placenta-enriched LincRNAs MIR503HG and LINC00629 decrease migration and invasion potential of JEG-3 cell line
- Idenficação de marcadores moleculares regulados pelo mecanismo de metilação em linhagens tumorais de cabeça e pescoço
- Bichemical and genetic analysis of butyrylcholinesterase (BChE) in a family, due to prolonged neuromuscular blockade after the use of succinylcholine
- Análise mutacional dos genes Col1a1 e Col1a2 em pacientes com suspeita clínica de osteogênese imperfeita
- 1031-1034delTAAC (Leu125Stop): a novel familial UBE3A mutation causing Angelman syndrome in two siblings showing distinct phenotypes
- Analysis of expression and methylation regulation of th MGC16121 and CR596471 genes and neighbor microRNAs
- Mutational screening in the LDLR gene among patients presenting familial hypercholesterolemia in the Southeast of Brazil
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
