Syndromic - Globe Thesis

Keyword [Syndromic] Result: 21 - 40 \| Page: 2 of 10
21.	Genetic Analysis Of The Candidate Genes Responsible For Non-syndromic Cleft Lip With Or Without Cleft Palate In Chinese People
22.	Clinical Investigation Of A Huge Family With Autosomal Dominant Hereditary Non-syndromic Hearing Loss
23.	The Comparative Research Of Craniofacial Structural Characteristic Of Syndromic And Nonsyndromic Patients With Cleft Palate
24.	Molecular Finding In Two Chinese Families With Nonsyndromic Hearing Impairment
25.	Mutations In The GJB2 Gene In Henan Patients With Prelingual Non-syndromic Hearing Impairment
26.	Syndromic Classifications Of Endometriosis In Lingnan Area On Traditional Chinese Medicine
27.	Research On The Relationships Of The Effect On Contaminations And Health Caused By Climate Change
28.	Gene Localization And A Novel Mutation Identified For Non-syndromic Hearing Loss
29.	Association Studies On Susceptibility Loci (Gene) Of Two Types Of Non-syndromic Hearing Impairment
30.	The Application Of Syndromic Data In Influenza Surveillance Of JiangSu Province
31.	Analyzing The Hereditary Features And The DNA Mutations In A Large Pedigree With Non-sensoneural Hearing Loss
32.	A Case-control Study Of Non-syndromic Cleft Lip And Palate In Shanxi Province
33.	The Study On The Correlation Between MSX1 Gene Exon2 And 3'non-coding Region Mutation And NSCL/P
34.	The Molecular Aetiology Study In Non-syndromic Hearing Impairment
35.	Optimization And Application Of Genetic Diagnostic System For Hereditary Nonsyndromic Hearing Loss
36.	Mutation Maps Drawing And Analysis Of Common Deafness Genes Among Non-syndromic Hearing Loss In Northwest China
37.	Backtrack Study Of Professor Zhouzhongying's Asthma Cases Based On A New Syndromic Etiology Theory
38.	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
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.	Frequency Of Chromosome 22q11.2 Microdeletion In Sporadic Non-syndromic Conotruncal Heart Defects By Multiplex Ligation-dependent Probe Amplification
<<First <Prev Next> Last>> Jump to