Microdeletion - Globe Thesis

Keyword [Microdeletion] Result: 41 - 60 \| Page: 3 of 5
41.	The Research On Y Chromosome Microdeletion And Cytogenetic Analysis In Male Infertility Patients
42.	Study On CITED2Mutation And22q11Microdeletion In Patients With Congenital Heart Disease
43.	Exploration The Method Of Y Chromosome Microdeletion Detection By Multiple Displacement Amplification (MDA) And Multiple PCR
44.	Application Of Chromosome Microarray Investigated Fetuses With Common Urinary Abnormalities
45.	Application Of Chromosome Microarray Analysis (CMA) Investigated33Patients With Congenital Cleft Lip And Palate
46.	Study On The Associations Between ESR2Gene Polymorphisms And Male Infertility Disease In Henan Han Population
47.	Study On The Relationship Between Y Chromosome Microdeletions And Male Infertility
48.	Analysis Of Y Chromosome AZF Region Microdeletions In Infertile Males
49.	Molecular Genetic Diagnosis For Fetus With Congenital Heart Disease
50.	Chromosome Alterlation,Y Chromosome Microdeletion And CDK2 Gene Analysis In Non-obstructive Azoospermia
51.	Study On Prenatal Diagnosis Using Both Karyotyping And BoBs
52.	Study On Genetic Variation Detection And Genetic Laws Of AZF Region In Infertility Male With Spermatogenesis Impairment
53.	Exploratory Study Of Non-obstructive Azoospermia-related Genes Based On Clinical Genetic Diagnosis
54.	The Application Research Of NIPT For Fetal Chromosomal Abnormalities And Functional Analysis Of GUCY2D Gene Mutations
55.	Establishment And Application Of Chromosomal Copy Number Variations Detection Based On High-throughput Sequencing
56.	Clinical Research On The Role Of Y Chromosome Microdeletion Detection In Male Infertility Diagnosis And Treatment And The Relationship Between It And Sex Hormone
57.	Application Study Of SNP Microarray In Spontaneous Abortion And Fetal Nervous System Abnormality
58.	Application Of Microdeletion And Microduplication Syndromes Detection Based On Next Generation Sequencing In The Prenatel Diagnosis
59.	Clinical Manifestations And Gene Analysis Of Dyschondroplasia And Chromosome 22q11 Microdeletion Syndrome
60.	Genotype And Clinical Phenotypic Research On A Boy Of Williams Syndrome
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