Tarkoititko:
segment nerve » segmental nerve (Laajenna hakua), augment nerve (Laajenna hakua), segmental nerves (Laajenna hakua)
crest drive » crest drives (Laajenna hakua), crest derived (Laajenna hakua), forest drive (Laajenna hakua)
system dias » system dan (Laajenna hakua), system dcs (Laajenna hakua), system dcus (Laajenna hakua)
genet nerve » genes serve (Laajenna hakua), bent nerve (Laajenna hakua), genital nerve (Laajenna hakua)
17 segment » _ segment (Laajenna hakua), a segment (Laajenna hakua), a1 segment (Laajenna hakua)
nerve cat » nerve can (Laajenna hakua), nerve ct (Laajenna hakua), nerve cut (Laajenna hakua)
cat diets » fat diets (Laajenna hakua), salt diets (Laajenna hakua), fad diets (Laajenna hakua)
case dis » case disc (Laajenna hakua), case did (Laajenna hakua), case di (Laajenna hakua)
i crest » i crestr (Laajenna hakua), _ crest (Laajenna hakua), a crest (Laajenna hakua)
j genet » j gentet (Laajenna hakua), j gene (Laajenna hakua), j genes (Laajenna hakua)
Näytetään 1 - 20 yhteensä 21 tuloksesta haulle '(( i crest drive system dias ) OR ((( j genet nerve case dis ) OR ( 17 segment nerve cat diets ))))', hakuaika: 1,27s Tarkenna hakua
Genetic Variation in Toll-Interacting Protein Is Associated With Leprosy Susceptibility and Cutaneous Expression of Interleukin 1 Receptor Antagonist
Pre-miR-146a (rs2910164 G>C) Single Nucleotide Polymorphism Is Genetically and Functionally Associated with Leprosy

Distinct clinical, neuroimaging and genetic profiles of late-onset cobalamin C defects (cb1C): a report of 16 Chinese cases
Triggers for Autism: Genetic and Environmental Factors

Use of Short Tandem Repeat Sequences to Study Mycobacterium leprae in Leprosy Patients in Malawi and India
Unusual multisystemic involvement and a novel BAG3 mutation revealed by NGS screening in a large cohort of myofibrillar myopathies

Late infantile metachromatic leukodystrophy: Clinical manifestations of five Taiwanese patients and Genetic features in Asia
Twenty-nine Cases of Enterovirus-D68–associated Acute Flaccid Myelitis in Europe 2016: A Case Series and Epidemiologic Overview

Biallelic SCN2A Gene Mutation Causing Early Infantile Epileptic Encephalopathy: Case Report and Review
Muscle-Eye-Brain Disease

Congenital Myasthenic Syndromes with Predominant Limb Girdle Weakness
Cluster headache

Selective cognitive and psychiatric manifestations in Wolfram Syndrome
Dominant optic atrophy

Mitochondrial genome variation in male LHON patients with the m.11778G > A mutation
Ocular manifestations in Gorlin-Goltz syndrome

Hereditary sensory neuropathy type I
Autosomal dominant cerebellar ataxia type I: A review of the phenotypic and genotypic characteristics

Vanishing White Matter Disease in a Spanish Population
Vitamin K Antagonist Warfarin for Palliative Treatment of Metachromatic Leukodystrophy, A Compassionate Study of Four Subjects

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