Nonsyndromic - Globe Thesis

Keyword [Nonsyndromic] Result: 81 - 100 \| Page: 5 of 6
81.	A Study Of Common Deafness Genes Using The Combination SNPscan And Sanger Sequencing In Nonsyndromic Hearing Loss Patients Of Minority In Northwest China And Mutation Analysis Of 9 Uncommon Deafness Genes Using SNPscan
82.	Association Study Of JARID2 Polymorphisms And Environmental Risk Factors With Nonsyndromic Orofacial Clefts
83.	Application Of Linked-Read Sequencing For Genome-wide Analysis In A Chinese Family With Nonsyndromic Cleft Lip And Palate And Treatment Analysis Of Moderate And Severe Maxillary Hypoplasia Using Le Fort ? Osteotomy
84.	The TPM1 And VANGL Polymorphisms And Nonsyndromic Orofacial Clefts Susceptibility In A Chinese Han Population
85.	Genome-wide Association Study Of Nonsyndromic Cleft Lip With Cleft Palate In Chinese Han Population
86.	Associations Of Genetic Variants In Endocytic Trafficking Of EGFR Super Pathway With Risk Of Nonsyndromic Cleft Lip With Or Without Cleft Palate
87.	Clinical Manifestation And Pathogenic Gene Analysis Of Inherited Nonsyndromic Ichthyoses
88.	Analysis Of The 12SrRNA Mutations In Patients With Nonsyndromic Hearing Impairment In Xinjiang Area
89.	A Pilot Study Of Differential Genes In Nonsyndromic Cleft Lip With Cleft Lip With Or Without Cleft Palate(NSCL/P) By Expression Microarray
90.	Statistics And Analysis Of Clinical Data Of 1749 Cases With Nonsyndromic Cleft Lip And Palate
91.	Association Between Forhead Box E1 Polymorphisms And Nonsyndromic Cleft Lip With Or Without Cleft Palate Risk:A Meta-analysis
92.	Association Between GWAS SNPs And Nonsyndromic Cleft Lip With Or Without Cleft Palate In Chinese Population
93.	RNA Sequencing Profiles Reveal Prenatal Biomarkers And Pathogenesis Of Nonsyndromic Cleft Lip With Palate
94.	Study And Application Of New Diagnostic Techniques On Genetic Deafness Genes And Molecular Genetic Study On A Family With Nonsyndromic Deafness
95.	Associations Of SNPs In MicroRNA Processing Genes And MSX1 With Nonsyndromic Oral Clefts Susceptibility
96.	Autophagy Is Involved In The Premature Calvarial Ossification In Nonsyndromic Craniosynostosis
97.	The Study On Whole Exome Sequencing Of Deafness Gene In Pedigrees Of Non-syndromic Hearing Loss In Guangxi Region
98.	Pathogenesis Of Digenic Variants In Nonsyndromic Hearing Loss
99.	Study On Molecular Genetic Pathogenic Factors And Genetic Counseling In Families With Non-syndromic Hereditary Deafness
100.	Clinical And Genetic Characteristics Of USH2A-associated Nonsyndromic Retinitis Pigmentosa And Usher Syndrome Type ?
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