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《AmericanJournalofHumanGenetics》期刊第58页200条数据 

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《American Journal of Human Genetics》期刊第58页

200条数据

https://www.zhangqiaokeyan.com/american-journal-human-genetics

1.《Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249135.html

2.《A Connective Tissue Disorder Caused by Mutations of the Lysyl Hydroxylase 3 Gene》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249136.html

3.《Recurrent CNVs Disrupt Three Candidate Genes in Schizophrenia Patients》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249137.html

4.《Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249138.html

5.《Population-Based Genome-wide Association Studies Reveal Six Loci Influencing Plasma Levels of Liver Enzymes》

genetics_thesis/040004249139.html

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-

6.《The H Syndrome Is Caused by Mutations in the Nucleoside Transporter hENT3》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249140.html

7.《Comparing Algorithms for Genotype Imputation》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249141.html

8.《Reply to Marchini and Howie》

genetics_thesis/040004249142.html

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-

9.《Announcements》

genetics_thesis/040004249143.html

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-

10.《HLA-DRB1?0401 and HLA-DRB1?0408 Are Strongly Associated with the Development of Antibodies against Interferon-β Therapy in Multiple Sclerosis》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249144.html

11.《This Month in The Journal》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249145.html

12.《This Month in Genetics》

genetics_thesis/040004249146.html

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-

13.《Victor Almon McKusick, MD, 1921–2008, In Memoriam》

genetics_thesis/040004249147.html

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-

14.《The DNA Wars: Part I》

genetics_thesis/040004249148.html

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-

15.《A Short History of the American Society of Human Genetics》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249149.html

16.《Methods for Detecting Associations with Rare Variants for Common Diseases: Application to Analysis of Sequence Data》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249150.html

17.《A Genome-wide Analysis of Admixture in Uyghurs and a High-Density Admixture Map for Disease-Gene Discovery》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249151.html

18.《Adaptive Evolution of UGT2B17 Copy-Number Variation》

genetics_thesis/040004249152.html

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-

19.《The Population Reference Sample, POPRES: A Resource for Population, Disease, and Pharmacological Genetics Research》

genetics_thesis/040004249153.html

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-

20.《Runs of Homozygosity in European Populations》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249154.html

21.《Optimized Allotopic Expression of the Human Mitochondrial ND4 Prevents Blindness in a Rat Model of Mitochondrial Dysfunction》

genetics_thesis/040004249155.html

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-

22.《DYRK1A-Dosage Imbalance Perturbs NRSF/REST Levels, Deregulating Pluripotency and Embryonic Stem Cell Fate in Down Syndrome》

genetics_thesis/040004249156.html

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-

23.《Genome-wide SNP-Based Linkage Scan Identifies a Locus on 8q24 for an Age-Related Hearing Impairment Trait》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249157.html

24.《C-Terminal Deletions in the ALAS2 Gene Lead to Gain of Function and Cause X-linked Dominant Protoporphyria without Anemia or Iron Overload》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249158.html

25.《FASTKD2 Nonsense Mutation in an Infantile Mitochondrial

Encephalomyopathy Associated with Cytochrome C Oxidase Deficiency》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249159.html

26.《Announcements》

genetics_thesis/040004249160.html

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-

27.《A Mutation in HOXA2 Is Responsible for Autosomal-Recessive Microtia in an Iranian Family》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249161.html

28.《A Bayesian Measure of the Probability of False Discovery in Molecular Genetic Epidemiology Studies》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249162.html

29.《Characterization of Apparently Balanced Chromosomal Rearrangements from the Developmental Genome Anatomy Project》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249163.html

30.《This Month in The Journal》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249164.html

31.《This Month in Genetics》

genetics_thesis/040004249165.html

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-

32.《An Algorithm for Inferring Complex Haplotypes in a Region of Copy-Number Variation》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249166.html

33.《Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubert Syndrome》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249167.html

34.《WW-Domain-Containing Oxidoreductase Is Associated with Low Plasma HDL-C Levels》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249168.html

35.《Maternally Inherited Birk Barel Mental Retardation Dysmorphism Syndrome Caused by a Mutation in the Genomically Imprinted Potassium Channel KCNK9》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249169.html

36.《A Comparative Analysis of the Genetic Epidemiology of Deafness in the United States in Two Sets of Pedigrees Collected More than a Century Apart》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249170.html

37.《Evolutionary Forces Shape the Human RFPL1,2,3 Genes toward a Role in Neocortex Development》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249171.html

38.《HLA-DRB1?0401 and HLA-DRB1?0408 Are Strongly Associated with the Development of Antibodies against Interferon-β Therapy in Multiple Sclerosis》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249172.html

39.《Extensive Copy-Number Variation of the Human Olfactory Receptor Gene Family》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249173.html

40.《ATM Gene Mutations Result in Both Recessive and Dominant Expression Phenotypes of Genes and MicroRNAs》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249174.html

41.《Pathogenic Mitochondrial DNA Mutations Are Common in the General Population》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249175.html

42.《Germline Mutations and Variants in the Succinate Dehydrogenase Genes in Cowden and Cowden-like Syndromes》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249176.html

43.《Class-Specific Correlations of Gene Expressions: Identification and Their Effects on Clustering Analyses》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249177.html

44.《Impairment of SLC17A8 Encoding Vesicular Glutamate Transporter-3, VGLUT3, Underlies Nonsyndromic Deafness DFNA25 and Inner Hair Cell Dysfunction in Null Mice》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249178.html

45.《Announcements》

genetics_thesis/040004249179.html

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-

46.《Congenital Joint Dislocations Caused by Carbohydrate Sulfotransferase 3 Deficiency in Recessive Larsen Syndrome and Humero-Spinal Dysostosis》

原文链接:https://www.zhangqiaokeyan.com/academic-journal-foreign-pmc_american-journal-human-genetics_thesis/040004249180.html

47.《Neuropsychological Endophenotype Approach to Genome-wide Linkage Analysis Identifies Susceptibility Loci for ADHD on 2q21.1 and 13q12.11》

《AmericanJournalofHumanGenetics》期刊第58页200条数据 

《AmericanJournalofHumanGenetics》期刊第58页200条数据https://www.zhangqiaokeyan.com/american-journal-human-genetics1.《MutationsinLPIN1CauseRecurrentAcuteMyoglobinuriainChi
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