Chromosomal Abnormalities - Globe Thesis

Keyword [Chromosomal Abnormalities] Result: 41 - 60 \| Page: 3 of 4
41.	A General Analysis On The Result Of Patients With Multiple Myeloma By Fluorescence In Situ Hybridization-a Report Of 100 Cases
42.	The Application Value Of Noninvasive Prenatal Testing In The Detection Of Fetal Chromosomal Abnormalities In Ningxia
43.	The Value Of First-trimester Ultrasound Screening And Multiple Indications In The Diagnosis Of Fetal Chromosomal Abnormalities
44.	The Use Of Whole-genome Sequencing To Expand Diatgnosis Of Chromosomal Abnormalities For Couples With Recurrent Pregnancy Loss And Their Impacts On Meiotic Segregation Patterns
45.	The Application Research Of NIPT For Fetal Chromosomal Abnormalities And Functional Analysis Of GUCY2D Gene Mutations
46.	The Establishment And Evaluation Of High-throughput Sequencing Method Based On Single Cell Whole-genome Amplification To Simultaneously Detecting Point Mutation And Copy Number Variation
47.	Screening,Identification Of Pathogenic Mutations And Karyotype Analysis Of Premature Ovarian Insufficiency
48.	Analysis Of The Correlation Between Fetal Chromosomal Abnormalities And Missed Abortion
49.	Relationship Between Recurrent Spontaneous Abortion And Chromosomal Abnormalities
50.	Relationship Between Fetal Nuchal Translucency Thickness And Chromosomal Abnormalities
51.	The Application Of Free DNA In Maternal Blood In Prenatal Screening Of Fetal Chromosomal Abnormalities
52.	Analysis Of Etiology Of Premature Ovarian Insufficiency In Children And Adolescent
53.	The Application Value Of Fetal Nasal Bone Ultrasound Evaluation In Chromosomal Abnormality Screening
54.	Comparison Of The Detection Rate Of Fetal Chromosomal Abnormalities Using Different Prenatal Screening Strategies
55.	Retrospective Analysis Of The Relationship Between Abnormal Fetal Ultrasonic Markers And Chromosomal Abnormalities
56.	Comparison of the types and levels of genotoxin-induced chromosomal abnormalities in cultured human cells
57.	Utilization of fish for constitutional and acquired chromosomal abnormalities for diagnostic and prognostic purposes
58.	Clinical Genetic Analysis And Whole-exome Sequencing With Rare Variant Association Study Of Nonobstructive Azoospermia
59.	Genomic Aberrations Of Ph+ Chronic Myeloid Leukemia Patients With Additional Chromosomal Abnormalities
60.	Analysis Of Amniotic Fluid Chromosome Karyotype Results In 1857 Cases With Different Prenatal Diagnosis Indications
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