Font Size: a A A
Keyword [Mutation Screening]
Result: 61 - 80 | Page: 4 of 6
61. Mutation Screening And Genetical Research Of Congenital Tooth Agenesis
62. Gene Mutation Screening Of A Family With Bardet-Biedl Syndrome
63. Gene Mutation Screening Of A Family With Paget’s Disease Of Bone And Candidate Genes Fuction Study
64. Association Study Between Autism And CORO2B And Mutation Screening For PAK2Gene In Autism From Chinese Population
65. Mutation Screening For An Idiopathic Generalized Epilepsies Pedigree By Exome Sequencing
66. Mutation Screening For Causative Gene In A Vascular Ehler-Danlos Syndrome Family
67. Mutation Screening Of BIGH3Gene In A Chinese Family With Granular Corneal Dystrophies
68. Mutation Screening Of Two Notch Signaling Pathway Related Genes And The Relationship To Simple Congenital Heart Disease
69. The Mutation Screening Of LKB1Gene In Familial Peutz-jeghers Syndrome Patients
70. STK11/LKB1Gene Mutation Screening And Proteomic Analysis Of Chinese PJS Patients
71. Gene Mutation Screening Of A Family With Retinitis Pigmentosa And Acropathy
72. Mutation Screening Of Candidate Genes In A Chinese Pedigree With Autosomal Dominant Hereditary Non-syndromic Auditory Neuropathy Spectrum Disorder And Study Of Development Of NELL2in Postnatal Mouse Cochlea
73. Screening The Mutation Of CHN1in Sporadic Duane Retraction Syndrome In Chinese Population
74. Mutation Screening Of SLC20A2, PDGFRB And PDGFB Genes In Southern Han Chinese Patients With Idiopathic Basal Ganglia Calcification And Analysis Of Their Clinical Characteristics
75. Identification Of The Novel Mutation IVS4ins6kb And Its Application In The Molecular Diagnosis Of NICCD Patients: Based On CDNA Cloning Analysis Of SLC25A13Gene In Peripheral Blood Lymphocytes
76. MPZ Gene Mutation Detection And The Phenotype Analysis In Chinese CMT Patients
77. Genetic Epidemiology Investigation And SCN5A Gene Mutation Screening In Familial Brugada Syndrome
78. Genome Editing Of Zebrafish Hoxb4 Gene Using CRISPR/Cas9 System And Its Mutant Screening
79. MLPA And DHPLC Technology Platform Based Pathogenic APC Gene Mutation Screening Of Familial Adenomatous Polyposis Predigrees And Analysis Of Mutation Molecular Mechanism
80. Clinical Features And Cognitive Function In The Children With Benign Childhood Epilepsy With Centro-temporal Spikes And GRIN2A Mutation Screening
  <<First  <Prev  Next>  Last>>  Jump to