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Keyword [Positional]
Result: 1 - 20 | Page: 1 of 10
1.
Mapping And Cloning Of Dentinogenesis Imperfecta Type â…¡
2.
A Novel Gene Is A Positional Candidate For Autosomal Recessive Polycystic Kidney Disease(ARPKD)
3.
Molecular Cloning And Functional Analysis Of A Novel Liver-related Putative Tumor Suppressor Gene (LPTS) With Telomerase Inhibitor Activity
4.
The Basic Study Of Vector And Target Site On The Therapy Of Marfan Syndrome By RNA Interference
5.
Mapping Of Pathogenic Gene In Three DGI-â…¡ Families
6.
Identification The Loci For Porokeratosis Palmaris Plantaris Et Disseminata And Disseminated Superficial Porokeratosis And Cloning The Gene Of Disseminated Superficial Porokeratosis
7.
Molecualr Genetics Of Klippel-Trenaunay Syndrome And Long QT Syndrome
8.
Refined Mapping Of Smith-Fineman-Myers Syndrome And Exclusion Of GPC3,GPC4,MST4,SMARCA1,GPCR2 And Glud2 As Candidate Genes
9.
Studies On The Identification Of The Objective Mice's Differentia Expressing Gene Affected By α-amanitin And The Drug Screening Of α-amanitin Resistence
10.
The Study On Pathogenic Gene Of Hereditary Progressive Cortical Cataract
11.
Positional Cloning And Functional Study Of Susceptibility Genes Of Type 2 Diabetes In Han People Of North China
12.
Chromosomal Localization Of Cat-like Cry And Mental Retardation In 5p Deletion Syndromes And Isolation Of ESTs From Related Regions
13.
Gene Mapping Of The Adult-form Autosomal Dominant Inherited Neuronal Ceroid-lipofuscinosis
14.
Fine Mapping Of The Regions With High LOH Frequencies And The Regions Related To Metastasis In Sporadic Colorectal Cancer And Filtrating Of Candidate Genes
15.
The Molecular Genetic Basis For Hereditary Late-onset Hearing Impairment
16.
Search For Susceptibility Genes Of Type 2 Diabetes In The Chinese
17.
The Positional Cloning Of A Complex Nervous System Disease From A Chinese Pedigree
18.
Clinical Manifestation And Maneuver Repositioning Therapy For Benign Paroxysmal Positional Vertigo
19.
Mapping And Positional Cloning The Causative Genes In Chinese Pedigrees With Non-syndromic Hereditary Hearing Impairment
20.
Disease-causing Gene Identification Of Human Juvenile Macular Dystrophy
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