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Keyword [genetic etiology]
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1. Analysis Of Genetic Etiology Of Nocturnal Frontal Lobe Epilepsy
2. The Clinical And Genetic Etiology Study Of Infantile Spasms
3. Whole Exome Sequencing Identifying Genetic Etiology Of Congenital Scoliosis In Chinese Han Population
4. Exploration Of Genetic Etiology For30Patients With Disorders Of Sex Development
5. Genetic Etiology Study Of 68 Short Stature Patients By Targeted Next-generation Sequencing
6. Exploration Of Genetic Etiology For The 45,X And 46,XX Male Patients With Disorder Of Sexual Development
7. Genetic Etiology Of Hedgehog Signaling Pathway And Scoliosis
8. A Series Of Studies On Prenatal Investigation And Diagnosis Of Genetic Etiology With Congenital Cleft Lip And Palate
9. The Investigation Of Genetic Etiology Of Unexplained Intellectual Disability/Global Developmental Delay
10. A Study On Pathogenic Gene Mutations In Patients With Premature Ovarian Insufficiency
11. Study On The Genetic Etiology Of Connective Tissue-related Genes And Congenital Scoliosis
12. Etiological Study Of Short Fetal Limbs In The First And Second Trimester And Noninvasive Prenatal Screening Of Fetal Achondroplasia
13. Molecular Genetics Etiology Study Of Children With General Developmental Delay/mental Retardation
14. Whole-Exome Sequencing Analysis Of Familial Chiari Malformation Type ? And Clinical/radiographic Study Of Chiari Malformation Type ?/scoliosis
15. Studies On Genetic Etiology Of Autism Spectrum Disorder And Neurological Mechanisms Underlying Cognitive Impairment Related To SH2B1 Gene
16. Genetic Etiology Of Oblique Vaginal Septum Syndrome
17. Genetic Etiology Of Patients With Disorders Of Sex Development
18. Preliminary Study On The Clinical Subtypes And Their Molecular Genetic Etiology Of Peutz-Jeghers Syndrome
19. Whole Exome Sequencing Of Seven Families With Acrodysostosis Analysis Of Genetic Etiology
20. Study Of Genetic Etiology Of Whole Exome Sequencing In Fetus With Ultrasound Structural Abnormal And In Family With Rare Disease
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