Font Size:
a
A
A
Keyword [pathogenic gene]
Result: 121 - 139 | Page: 7 of 7
121.
Study Of The Effects Of Carpenter Syndrome Pathogenic Gene,Megf8,on Synaptic System Using Drosophila Model
122.
Clinical Investigation,Pathogenic Gene Detection And Multi-omics Analysis Of An Undiagnosed Rare Genetic Disease
123.
Identification Of Pathogenic Gene Mutations In Chinese Alport Syndrome Patients
124.
Study On The Mechanism Of BMS-470539 Activation Of MC1R To Regulate The Treatment Of Vitiligo
125.
Analysis Of Environmental And Genetic Factors Of Clinical Characteristics Of Patients With Moyamoya Disease And Identification And Functional Study Of New Pathogenic Gene CAPN1
126.
Identification And Functional Study Of A Pathogenic Gene Associated With High Myopia In Uyghurs Based On Epidemiological Survey And Whole-exome Sequencing
127.
Study On Gene Diagnosis,Novel Pathogenic Gene Mutation And Gene Methylation Of Alport Syndrome
128.
Study On Clinical Characteristics Of Alzheimer's Disease Patients With And Without Pathogenic Gene Mutation
129.
Study On The Function And Regulation Mechanism Of Gout Pathogenic Gene PLAA In Monocytes
130.
Explore The Pathogenic Gene Of A Case Of Familial Eruptive Vellus Hair Cysts
131.
Pathogenic Gene Mutation And Molecular Mechanism Of An X-linked Hypohidrotic Ectoderm Dysplasia Family
132.
Genetic Verification Of The Pathogenic Gene Of A New Mutation In ADAR1 In Hereditary Dyschromes Symmetries
133.
Family Pathogenic Gene Mutations And Disease Progression Clinical Indicator Analysis For ADPKD Patients In Southwestern Shandong
134.
Study On Pathogenic Variation Of Single Gene Disease In Hohhot
135.
Screening Pathogenic Genes Of Right Heart Failure And Prediction Of Potential Therapeutic Drugs Based On Bioinformatics Analysis
136.
Analysis Of Clinical Characteristics And Mutation Of Pathogenic Gene In One Netherton Syndrome Family
137.
The Identification Of A New Pathogenic Gene UGDH In Primary Microcephaly
138.
Clinical Characteristics And Pathogenic Gene Identification Of Four Patients With Suspected Thrombophilia
139.
Fine Mapping Of Pathogenic Gene In A Porcupine Model Of Spontaneous Syndromic Deafness Associated With Pigmentation Abnormalities
<<First
<Prev
Next>
Last>>
Jump to