Linkage of the LW blood group locus with the complement C3 and Lutheran blood group lociEvidence by expression analysis of candidate genes for congenital heart defects in the NF1 microdeletion intervalIdentification of VAV2 on 9q34 and its exclusion as the tuberous sclerosis gene TSC1Cloning and evaluation of RALGDS as a candidate for the tuberous sclerosis gene TSC1Cloning and chromosome assignment of the human CDX2 geneSequence of full length cDNA for human S-adenosylhomocysteine hydrolaseFounder mutation(s) in the RSPH9 gene leading to primary ciliary dyskinesia in two inbred Bedouin familiesGenome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease2E4/Kaptin (KPTN)--a candidate gene for the hearing loss locus, DFNA4Geographical structure of the Y-chromosomal genetic landscape of the Levant: a coastal-inland contrastRefined geographic distribution of the oriental ALDH2*504Lys (nee 487Lys) variantWide disparity in genetic admixture among Mexican Americans from San Antonio, TXFragile X syndrome: the FMR1 CGG repeat distribution among world populationsAssociation of linear growth impairment in pediatric Crohn's disease and a known height locus: a pilot studyA genome-wide association study of autism reveals a common novel risk locus at 5p14.1Identification of association of common AGGF1 variants with susceptibility for Klippel-Trenaunay syndrome using the structure association programValidation study of genetic associations with coronary artery disease on chromosome 3q13-21 and potential effect modification by smokingThe reduced folate carrier (SLC19A1) c.80G>A polymorphism is associated with red cell folate concentrations among womenImportance of Genetic Studies in Consanguineous Populations for the Characterization of Novel Human Gene FunctionsSpinal muscular atrophy: from gene discovery to clinical trialsTumor necrosis factor and interleukin-6 gene polymorphisms and endometriosis risk in Asians: a systematic review and meta-analysisTrans-ethnic meta-analysis identifies common and rare variants associated with hepatocyte growth factor levels in the Multi-Ethnic Study of Atherosclerosis (MESA).Studies on the subunit structure and molecular size of the human alcohol dehydrogenase isozymes determined by the different loci, ADH1, ADH2, and ADH3Antigenic analysis of the major human phosphoglucomutase isozymes: PGM1, PGM2, PGM3 and PGM4Biochemical genetics of the pentose phosphate cycle: human ribose 5-phosphate isomerase (RPI) and ribulose 5-phosphate 3-epimerase (RPE)Studies on human erythrocyte inorganic pyrophosphataseAconitase polymorphism in manHaplotype analysis of three polymorphisms of the COL2A1 gene and associations with generalised radiological osteoarthritisPhylogeographic patterns of mtDNA reflecting the colonization of the Canary IslandsSub-unit structure of soluble and mitochondrial malic enzyme: demonstration of human mitochondrial enzyme in human-mouse hybridsThe hereditary elliptocytoses: clinical and linkage dataA multistep process for the dispersal of a Y chromosomal lineage in the Mediterranean areaMolecular cloning, functional characterization and genomic organization of four alternatively spliced isoforms of the human organic cation transporter 1 (hOCT1/SLC22A1)Y chromosome and mitochondrial DNA characterization of Pasiegos, a human isolate from Cantabria (Spain)Methylenetetrahydrofolate reductase (MTHFR) allele frequencies in AmerindiansPhylogeography of the human mitochondrial haplogroup L3e: a snapshot of African prehistory and Atlantic slave tradeHaplotype analysis of the human alpha2-HS glycoprotein (fetuin) geneThe phylogeography of Y chromosome binary haplotypes and the origins of modern human populationsMitochondrial DNA variability in Russians and Ukrainians: implication to the origin of the Eastern SlavsMitochondrial DNA variability in Bosnians and Slovenians
P1433
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P1433
description
journal
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revista científica
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revue scientifique
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rivista scientifica
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vědecký časopis
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wetenschappelijk tijdschrift van John Wiley & Sons
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wissenschaftliche Fachzeitschrift
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مجلة
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वैज्ञानिक पत्रिका
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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Annals of Human Genetics
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P243
P3181
P356
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P1144
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P1160
Ann. Hum. Genet.
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P1250
P1277
P1476
Annals of Human Genetics
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P236
P243
P3181
P356
10.1111/(ISSN)1469-1809