Pesquisas alternativas:
central nerve » ventral nerve (Expandir a Pesquisa), central nervous (Expandir a Pesquisa), central neural (Expandir a Pesquisa)
crest nerve » treat nerve (Expandir a Pesquisa), crest derived (Expandir a Pesquisa), current nerve (Expandir a Pesquisa)
nerve cnase » nerve case (Expandir a Pesquisa), nerve cases (Expandir a Pesquisa), nerve cause (Expandir a Pesquisa)
genet nerve » genes serve (Expandir a Pesquisa), bent nerve (Expandir a Pesquisa), genital nerve (Expandir a Pesquisa)
nerve cyst » nerve cystic (Expandir a Pesquisa), nerve case (Expandir a Pesquisa), nerve cat (Expandir a Pesquisa)
j central » 1hfj central (Expandir a Pesquisa)
cyst dis » cyst due (Expandir a Pesquisa), cyst d (Expandir a Pesquisa), cyst dna (Expandir a Pesquisa)
j crest » _ crest (Expandir a Pesquisa), a crest (Expandir a Pesquisa), 5 crest (Expandir a Pesquisa)
j genet » j gentet (Expandir a Pesquisa), j gene (Expandir a Pesquisa), j genes (Expandir a Pesquisa)
nerve c » nerve cn (Expandir a Pesquisa), nerve co (Expandir a Pesquisa), nerve ct (Expandir a Pesquisa)
c due » c duke (Expandir a Pesquisa), _ due (Expandir a Pesquisa), 2 due (Expandir a Pesquisa)
A mostrar 1 - 20 resultados de 88 para a pesquisa '(((( j central nerve cyst dis ) OR ( j crest nerve cnase dis ))) OR ( j genet nerve c due ))*', tempo de pesquisa: 2.10seg Refinar resultados
Influence of Mitochondrial Genetics on the Mitochondrial Toxicity of Linezolid in Blood Cells and Skin Nerve Fibers
Genetic control of renin activity in the submaxillary gland of the mouse.

Secondary meningioma in a long-term survivor of atypical teratoid/rhabdoid tumour with a germline INI1 mutation
Monitoring activity-dependent bulk endocytosis with the genetically-encoded reporter VAMP4-pHluorin

High-Frequency Burst Vagal Nerve Simulation Therapy in a Natural Primate Model of Genetic Generalized Epilepsy
Strategy for genetic testing in Charcot-Marie-Disease

Genetic Hearing Loss Associated With Autoinflammation
Complete callosal agenesis, pontocerebellar hypoplasia, and axonal neuropathy due to AMPD2 loss

Synovial sarcoma of the spine: A report of three cases and review of the literature
Autosomal dominant burning feet syndrome

Midline axon guidance in the Drosophila embryonic central nervous system
Rat Na(V)1.7 loss-of-function genetic model: Deficient nociceptive and neuropathic pain behavior with retained olfactory function and intra-epidermal nerve fibers

Differential response of C57BL/6J mouse and DBA/2J mouse to optic nerve crush
Differential response of C57BL/6J mouse and DBA/2J mouse to optic nerve crush

Deletion of myeloid IRS2 enhances adipose tissue sympathetic nerve function and limits obesity
Ophthalmic manifestations in a Chinese family with familial amyloid polyneuropathy due to a TTR Gly83Arg mutation

Neurofibromatosis without Neurofibromas: Confirmation of a Genotype-Phenotype Correlation and Implications for Genetic Testing
Brain and ventricular volume in patients with syndromic and complex craniosynostosis

An Inherited Disorder With Splenomegaly, Cytopenias, and Vision Loss
Genetically induced abnormal cranial development in human trisomy 18 with holoprosencephaly: comparisons with the normal tempo of osteogenic–neural development

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