The incidence of alkaptonuria: a study in chemical individuality. 1902 [classical article]
about
On the ocular findings in ochronosis: a systematic review of literatureClinical Metabolomics: The New Metabolic Window for Inborn Errors of Metabolism Investigations in the Post-Genomic EraEnvironmental Chemical Assessment in Clinical Practice: Unveiling the Elephant in the RoomCharacterising the spectrum of autosomal recessive hereditary hearing loss in IranThe molecular basis of alkaptonuriaCharacterization of a fungal maleylacetoacetate isomerase gene and identification of its human homologueDirectional dominance on stature and cognition in diverse human populationsHistory and evolution of cytogeneticsDeveloping products for personalized medicine: NIH Research Tools Policy applicationsThe new field of 'precision psychiatry'.ApreciseKUre: an approach of Precision Medicine in a Rare Disease.Development of molecular genetics.Multiple sclerosis, vitamin D, and HLA-DRB1*15.Consulting the source code: prospects for gene-based medical diagnostics.An update on molecular genetics of Alkaptonuria (AKU).Consanguinity and its relevance to clinical genetics.Gene-environment interactions in human diseases.Genotype-environment interactions and their translational implications.Pharmacogenomic technologies: a necessary "luxury" for better global public health?Pharmacogenetics - five decades of therapeutic lessons from genetic diversity.Mechanotransduction Mechanisms for Intraventricular Diastolic Vortex Forces and Myocardial Deformations: Part 2.Defining and addressing the nutritional needs of populations.Cloning of the homogentisate 1,2-dioxygenase gene, the key enzyme of alkaptonuria in mouse.An overview of biochemical genetics.Cultural differences define diagnosis and genomic medicine practice: implications for undiagnosed diseases program in China.Inborn errors of metabolism: challenges and managementCytogenetics and the evolution of medical genetics.Metabolomics: unraveling the chemical individuality of common human diseases.The role of nutritional genomics in developing an optimal diet for humans.Statistical issues in quality control of proteomic analyses: good experimental design and planning.Alkaptonuria in France: past experience and lessons for the future.Overview of pharmacogenetics.The family history: the first genetic test, and still useful after all those years?The application of next-generation sequencing in the autozygosity mapping of human recessive diseases.Inborn errors of metabolism and expanded newborn screening: review and update.Human genetics in troubled times and places.Genomic Bayesian functional regression models with interactions for predicting wheat grain yield using hyper-spectral image dataXERODERMA PIGMENTOSUM. A BRIEF REPORT ON ITS GENETIC LINKAGE WITH ABO BLOOD GROUPS IN THE UNITED ARAB REPUBLIC.Cartilage biomarkers in the osteoarthropathy of alkaptonuria reveal low turnover and accelerated ageing.The molecular genetics of human monogenic diseases.
P2860
Q21260367-3C6E93A7-1A9D-4456-AB3D-A02F62034F9FQ26742050-107F3524-309A-4171-8F61-202C5E6D8542Q26768636-23CBD665-5013-44C0-AA19-A36DC2864AB2Q27317126-01613056-A479-44D7-8F7F-158E9BD11B90Q28118128-4E7FA5D8-C484-4126-ADE2-B8F0A0D7893EQ28118834-DAC5940D-3ABD-40AF-909E-D94C26030E76Q28646221-7F9F7521-9C45-4281-B9CC-23C7DA906708Q28651651-6B35A4E9-271E-4ABF-AF6B-1C57C8D748B0Q28749694-75F567C0-46FF-46D2-82D8-532E1475715DQ33560453-DA08F6AA-DC98-47C3-A84B-2F53FD73E25CQ33564599-075587FC-8A7E-4C03-93F0-0ABF0C1EE66BQ33746321-801F0B6F-7E70-4331-AC82-DA0E1AA83EDCQ33899907-65C91CC3-FDE3-435B-9F21-24F7C6242906Q34086825-46E40E73-2D08-4774-AFD6-B1FF1E270EB8Q34196817-C3A6E172-4C34-424F-98F3-942CC1846FC6Q34366023-BA1130E4-D35D-4232-90AF-50DE92241A39Q34407923-46BFF3A8-DE4B-4FBA-ACC7-D567EB17EBF6Q35024668-6794EBCD-57C8-4DB4-96BA-2CB27D7D1B72Q35219458-06D99C08-8335-4FEC-8DD1-7060471BCD4EQ35889619-F2CA18D4-6CE8-4123-BCD3-07DCC62EE942Q35901064-4F796304-D708-4116-BCAD-7388A5F6947AQ36291100-C098E4D5-8247-49DF-808C-EAAC7975EB28Q36850258-53E4C43D-9C02-4A25-A387-A91375BF5F98Q37144360-8A647182-3B14-4F93-A3A4-613EF5E23B75Q37149509-F61EDACF-11CC-48F0-848E-A93C61A9D1DAQ37199418-9EA4BEA3-AB02-492E-B50C-502880AFE2EFQ37222110-F781D65C-A4A2-40CE-850A-A04977D4CF73Q37384824-1467A906-B653-4FB3-921E-55331F2A8D8DQ37817617-C579B9D4-16B7-4C31-B2F1-85C02E764A56Q37836674-91592914-4446-4179-BE9E-0F952DC5DDF9Q37934608-326B0B14-F6CD-42B2-890B-2D21099E3C0DQ37938905-18CCE40F-59B5-4B3C-A87A-3AAE73145163Q37975105-7F59F6B9-89CE-4A34-8D7B-DFD425D811ABQ38125937-7340CD46-8F2D-43C3-A8CD-845D922955B9Q38167824-98B04090-14F6-40F6-8F9F-567E275B8BB6Q38644665-29D3A03C-E675-45EE-97AD-8F9E7738B944Q38645534-5B3AF02C-8389-4BDE-AD98-F49BDA07D712Q38987961-B4516012-DE72-4419-8C27-F7B0BE4AD11EQ39061550-F0E3A879-DD50-42C8-897A-874856812C38Q39499560-A1266F4F-7ABB-433B-BB5E-384EFE07D2EB
P2860
The incidence of alkaptonuria: a study in chemical individuality. 1902 [classical article]
description
2002 nî lūn-bûn
@nan
2002 թուականին հրատարակուած գիտական յօդուած
@hyw
2002 թվականին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
The incidence of alkaptonuria: ...... lity. 1902 [classical article]
@ast
The incidence of alkaptonuria: ...... lity. 1902 [classical article]
@en
The incidence of alkaptonuria: ...... lity. 1902 [classical article]
@nl
type
label
The incidence of alkaptonuria: ...... lity. 1902 [classical article]
@ast
The incidence of alkaptonuria: ...... lity. 1902 [classical article]
@en
The incidence of alkaptonuria: ...... lity. 1902 [classical article]
@nl
prefLabel
The incidence of alkaptonuria: ...... lity. 1902 [classical article]
@ast
The incidence of alkaptonuria: ...... lity. 1902 [classical article]
@en
The incidence of alkaptonuria: ...... lity. 1902 [classical article]
@nl
P3181
P1476
The incidence of alkaptonuria: ...... lity. 1902 [classical article]
@en
P2093
Archibald E Garrod
P304
P3181
P356
10.1016/S0140-6736(01)41972-6
P407
P577
2002-01-01T00:00:00Z