autosomal-dominant - Globe Thesis

Keyword [autosomal-dominant] Result: 41 - 60 \| Page: 3 of 10
41.	Study Of Molecular Mechanism Of Autosomal Dominant Nonsyndromic Hereditary Hearing Loss And Pfeiffer Syndrome
42.	Inhibiting Effect Of Rosiglitazone And Rapamycin Combination On Cystic Epithelial Cells In ADPKD And Its Mechanism
43.	RNAi-based Suppression Of Human RHO In A Mouse Model Of Autosomal Dominant Retinitis Pigmentosa
44.	Evaluation Of NOTCH3 Protein And GOM In The Pathological Mechanism Of Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts And Leukoencephalopathy (CADASIL)
45.	Mapping And Mutation Analysis For Hereditary Congenital Cataract In Chinese Families
46.	Tcm Triangular And Eupolyphaga Of The Polycystic Kidney Disease-lining Epithelial Cell Proliferation And Signal Transduction
47.	Molecular Genetics Of Hereditary Diseases. High Myopia And Eye Research
48.	Clinical Analysis And PAX6Gene Association Study Of A Chinese Family With Autosomal Dominant Congenital Aniridia
49.	The Study Of Loca Lization Of Autosomal Dominant Retinitis Pigmentosa Gene And Detection Of Mutation On Rhodopsin Gene
50.	Identification Of Disease Gene And Analysis Of Clinical And Genetic Features Of Multiple Familial Trichoepithelioma
51.	Role Of Transforming Growth Factor-betal In Pathogenesis Of Human Autosomal Dominant Polycystic Kidney Disease
52.	Role Of Insulin-like Growth Factor-1 In The Pathogenesis Of Autosomal Dominant Polycystic Kidney Disease
53.	Clinical Investigation Of A Huge Family With Autosomal Dominant Hereditary Non-syndromic Hearing Loss
54.	Clinical, Electrophysiological, Pathological And Genomic Study Of Hereditary Neuropathy With Liability To Pressure Palsies
55.	Mutation Detection In PKD1 Gene In Chinese Adpkd Families By Using PCR And DNA Sequencing
56.	Laparoscopic Management Of Autosomal Dominant Polycystic Kidney
57.	The Study Of Causative Genes In A Chinese Family With Autosomal Dominant Congenital Cataract
58.	1.Effects Of Intraocular Lenses Of Different Materials On Posterior Capsule Opacification: A Systematic Review 2.Screening Of Genes Causing Autosomal Dominant Lamellar Cataract In A Chinese Family
59.	Preliminary Study Of A Family With Ophthalmoplegia,Dysphagia And Facial Weakness
60.	Gene Mutation Pattern In A Chinese Family With Stargardt3-like Disease
<<First <Prev Next> Last>> Jump to