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Keyword [Non-syndromic]
Result: 21 - 40 | Page: 2 of 8
21. Mutations In The GJB2 Gene In Henan Patients With Prelingual Non-syndromic Hearing Impairment
22. Gene Localization And A Novel Mutation Identified For Non-syndromic Hearing Loss
23. Association Studies On Susceptibility Loci (Gene) Of Two Types Of Non-syndromic Hearing Impairment
24. Analyzing The Hereditary Features And The DNA Mutations In A Large Pedigree With Non-sensoneural Hearing Loss
25. A Case-control Study Of Non-syndromic Cleft Lip And Palate In Shanxi Province
26. The Study On The Correlation Between MSX1 Gene Exon2 And 3'non-coding Region Mutation And NSCL/P
27. The Molecular Aetiology Study In Non-syndromic Hearing Impairment
28. Optimization And Application Of Genetic Diagnostic System For Hereditary Nonsyndromic Hearing Loss
29. Mutation Maps Drawing And Analysis Of Common Deafness Genes Among Non-syndromic Hearing Loss In Northwest China
30. A Relative Study On The Patients With Non-syndromic Hereditary Hearing Loss Of GJB2 Gene Mutations And Kidney Deficiency And Blood Stasis In Uyghur And Han In Xinjiang
31. The Relativity Study Of The Mitochondrial Gene Mutation Of Non-syndromic Hearing Loss And Kidney Deficiency With Blood Stasis Type Of Uigur And Han
32. Frequency Of Chromosome 22q11.2 Microdeletion In Sporadic Non-syndromic Conotruncal Heart Defects By Multiplex Ligation-dependent Probe Amplification
33. Association Between Rs1805087 Polymorphisms Of MTR Gene And Non-syndromic Cleft Lip With Or Without Cleft Palate
34. Association Of MSX1 Genetic Polymorphism With Non-syndromic Cleft With Or Without Cleft Palate
35. Molecular Genetic Characterization Of Two Chinese Pedigrees With Aminoglycoside-induced And Non-syndromic Hearing Loss
36. Sequence Analysis Of The Complete Mitochondrial Genome And TRMU Gene Of Two Pedigrees With Hearing Impairment Associated With The 12S RRNA A827G Mutation
37. Sequence Analysis Of Mitochondrial 12S RRNA And TRNASer(UCN) Genes In Patients With Non-syndromic Hearing Loss
38. Mutational Analysis Of SLC26A5 IVS2-2A>G In Chinese Han Patients With Non-syndromic Hearing Loss
39. The Relativity Study Of The Mitochondrial Gene Mutation Of Non-syndromic Hearing Loss And Kidney Deficiency With Blood Stasis Type Of Uigur And Han
40. Sequence Analysis Of Mitochondrial 12s Rrna And Trnaser(ucn) Genes In Patients With Non-syndromic Hearing Loss
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