Spinal Muscular Atrophy - Globe Thesis

Keyword [Spinal Muscular Atrophy] Result: 21 - 40 \| Page: 2 of 4
21.	Gene Diagnosis Of DMD And SMA By Multiplex Ligation-dependent Probe Amplification Combined With DNA/cDNA Sequencing
22.	Gene Diagnosis Of Dmd And Sma By Multiplex Ligation-dependent Probe Amplification Combined With Dna/cdna Sequencing
23.	Fluorescence Quantitative Pcr In The Diagnosis Of Genetic Diseases
24.	Preliminary Randomised Crossover Clinical Study On Effect Of Mouse Nerve Growth Factor In Treating Childhood Spinal Muscular Atrophy
25.	The Gene Diagnosis Research Of Spinal Muscular Atrophy Using PCR-RFLP And MLPA
26.	Molecular Analysis Of Genes In5q13Region In Patients With Spinal Muscular Atrophy
27.	Clinical Characteristics Of Different Phenotypes In Children With Spinal Muscular Atrophy
28.	Genetic Testing And Clinical Application Of Hereditary Polycystic Kidney Disease And Spinal Muscular Atrophy
29.	Smn-1interacts With Uaf-1to Regulate Caenorhabditis Elegans Lifespan And Motor Function
30.	Application Of MLPA In Molecular Diagnosis And Prenatal Diagnosis Of Spinal Muscular Atrophy
31.	Establishment Of Urine-derived Cell Lines From SMA Patients And Exploration Of IPS Reprogramming And Direct Conversion
32.	The Tissue Expression Of NMNAT1 And SIRT1 In LCA Mice With Compound Heterozygote With NMNAT1 Mutation And A Novel Frameshift Mutation Of SMN1 Gene Cause Spinal Muscular Atrophy
33.	A-44G Transition In SMN2 Intron 6 Protects Patients With Spinal Muscular Atrophy
34.	Detection Of Copy Number Variation In Spinal Muscular Atrophy (SMA) And Duchenne Muscular Dystrophies (DMD) By Multiplex Ligation-dependent Probe Amplification-based Real-time PCR
35.	Molecular Detection Of Spinal Muscular Atrophy By MALDI-TOF MS&Preimplantation Genetic Diagnosis Of α-thalassemia SEA Deletion Utilizing Whole Genome Amplification And Short Fragment Gap-PCR Method
36.	A Large Chinese Family With A Novel Mutation In The TRPV4 Gene That Causes Congenital Distal SMA And Spondylometaphyseal Dysplasia
37.	Identification Of Pathogenic Point Mutations In Spinal Muscular Atrophy And Embryonic Therapy In SMA Mouse Using CRISPR/Cas9
38.	Analysis Of Natural History Of Spinal Muscular Atrophy In 117 Children
39.	Study Of Systemic Inflammation In A Mouse Model Of Spinal Muscular Atrophy
40.	Genetic Screening Of Spinal Muscular Atrophy(SMA) In Pregnant Women
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