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Keyword [autosomal-dominant]
Result: 21 - 40 | Page: 2 of 10
21. Genome-Wide Scanning For A Nonsyndromic Autosomal Dominant Deafness In A Six-Generation Family
22. Genome-Wide Scanning For A Nonsyndromic Autosomal Dominant Postaxial Polydactyly In A Six-Generation Family
23. Gene Mapping Of The Adult-form Autosomal Dominant Inherited Neuronal Ceroid-lipofuscinosis
24. The Molecular Genetic Basis For Hereditary Late-onset Hearing Impairment
25. Experimental Study On Celecoxib Treating Autosomal Dominant Polycystic Kidney Disease
26. Experimental Research On The Treatment Of Autosomal Dominant Polycystic Kidney Disease With PPARγ Agonists
27. RP33, A Novel Locus Of Autosomal Dominant Retinitis Pigmentosa; And A Complete Mutation Screening Of PRPF31 Gene In RP11 Linked Family
28. A Chinese Familial And Sporadic Cases With Congenital Fibrosis Of The Extraocular Muscles: Clinical And Molecular Genetic Study
29. Comparative Phosphoproteomic Analysis Of Autosomal Dominant Polycystic Kidney Disease
30. Arterial Function In Autosomal Dominant Polycystic Kidney Disease
31. Molecular Genetic Analysis Of Hereditary Eye Diseases
32. Experimental Study On Mycophenolate Mofetil Treating Autosomal Dominant Polycystic Kidney Disease
33. Gene Mapping Of Atrophia Maculosa Varioliformis Cutis
34. Analysis Of Clinical Features And Study Of Responsible Genes For The Chinese Retinitis Pigmentosa And Usher Syndrome Families
35. Molecular Cloning And Characterization Of Mtsarg1-β Mutation Detection Of Polycystic Kidney Disease Gene 1 (PKD1)
36. Gene Mapping And Analysis Of Candidate Genes In Three Chinese Families With Congenital Cataract
37. Gene Mapping Of Acne Inversa
38. Mapping And Positional Cloning The Causative Genes In Chinese Pedigrees With Non-syndromic Hereditary Hearing Impairment
39. Localization Of Genes For Inherited Skin Diseases And Hearing Loss And Mutational Studies
40. The Clincal Study And NOTCH3 Gene Mutation Of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts And Leukoencephalopathy (CADASIL)
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