European Human Genetics Conference 2007 June 16 – 19, 2007 ...
European Human Genetics Conference 2007 June 16 – 19, 2007 ...
European Human Genetics Conference 2007 June 16 – 19, 2007 ...
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Keyword Index 1<br />
Fronto-temporal dementia: P0640<br />
FSHD: P0741<br />
FTH: P0220<br />
FTL: P0220<br />
Functional analysis: C50<br />
Functional assay: P0565<br />
functional polymorphism: C13<br />
functional SNP: C72<br />
fundus albipunctatus: P0234<br />
FVIII: P1158<br />
FXN: P0739<br />
FXS: P0738<br />
FXTAS: P0121<br />
FZD4: P0742<br />
G bands: P0257<br />
G2-assay: P0304<br />
G6PD: P0743<br />
G72/G30 genes: P1014<br />
G743E mutation: P0645<br />
GABA receptor: P0974<br />
galactosemia: P0122<br />
GALNT3: P0730<br />
GALT: P0122<br />
γInterferon-gamma (IFN-: P0990<br />
Gap junction: P0744<br />
gastric cancer: P0522, P0551<br />
gastric intraepithelial neoplasias: P0578<br />
gastro-enterology: P0146<br />
GATA4: P0318<br />
Gaucher: P1408<br />
Gaucher disease: P0123, P1406<br />
GDAP1: P0975<br />
GEFS+: P0976<br />
Gender: P1117<br />
gene: P1331<br />
gene alterations: P0296<br />
gene classifier: P1300<br />
gene conversion: P0637, P09<strong>16</strong><br />
Gene defect: P0669<br />
gene delivery: P1407<br />
Gene dosage: C33<br />
gene expression: P0552, P1254, P1255, P1256,<br />
P1282, P1289<br />
Gene expression analysis: P1233<br />
gene expression patterns: S<strong>19</strong><br />
gene expression profiles: P0785<br />
gene expression profiling: P0766<br />
gene expression variation: P1151<br />
Gene Mutations: P0731<br />
gene polymorphism: P0228, P0265, P0537, P0977,<br />
P1180, P1299<br />
gene rearrangements: P0078<br />
gene regulation: P0661, P1247<br />
gene therapy: C<strong>19</strong>, P0266, P1397<br />
gene transfer: C59<br />
gene-environment interaction: P1159<br />
genes: P0745<br />
genetic: P0027, P0902, P1257<br />
genetic alterations: P0608<br />
genetic association: P0948, P1022<br />
genetic association studies: P1<strong>16</strong>6<br />
Genetic counselling: P00<strong>16</strong>,P0124, P0145, P0148,<br />
P0152, P0402, P0627, P1332, P1333, P1334, P1335,<br />
P1336, P1337, P1338, P1342, P1371, P1381, P1385<br />
genetic counsellors: P1339, P1340<br />
Genetic databases: P1258<br />
genetic deafness: P1355<br />
genetic disorder: P0553<br />
genetic diversity: P1179<br />
genetic epidemiology: P1<strong>16</strong>0, P1<strong>16</strong>1<br />
Genetic heterogeneity: P1270<br />
genetic information: P1341<br />
genetic landscapes: P1<strong>16</strong>2<br />
genetic linkage: P1076<br />
Genetic linkage analysis: C40<br />
genetic mapping: P1056<br />
genetic polymorphism: P0623, P0898, P09<strong>19</strong>, P0929,<br />
P0978, P1<strong>16</strong>3<br />
genetic predisposition: P1047, P1096, P1342<br />
genetic profiling: S03<br />
Genetic Route Maps: P1343<br />
genetic screening: P0873<br />
genetic service: P1306<br />
genetic services: P1321, P1326<br />
genetic structure: P1207<br />
Genetic test: P0554, P1344<br />
Genetic testing: C81, P0099, P0669, P1307, P1308,<br />
P1345, P1346, P1347, P1350, P1361, P1383<br />
genetic variants: P0915<br />
genetic variation: P1<strong>16</strong>4<br />
genetics: P0530, P1128<br />
genetics and public policy: P1348<br />
genetics education: C83, P1317<br />
genetics in clinical practice: P1317<br />
<strong>Genetics</strong> Services: P1349<br />
genodermatoses: C59<br />
genome: S03<br />
Genome regulation: P0518<br />
genome-scan: P0918, P0923, P0935<br />
genomewide: P0934<br />
genome-wide analysis: P0909<br />
genome-wide association: C46<br />
Genome-wide association study: P0979<br />
genome-wide heterozygosity: C47, P1<strong>16</strong>5<br />
Genome-wide Linkage & Association: P1<strong>19</strong>8<br />
Genomewide scan: P0970, P1<strong>16</strong>6<br />
genomic data banks: P1246<br />
Genomic disorders: C74<br />
genomic imprinting: P0340, P0980<br />
genomic instability: P0576<br />
genomic profiling: P1259<br />
Genomic Services: P1360<br />
Genomics: P1388<br />
Genotype: P0223<br />
genotype-phenotype: P0825, P0940, P1052<br />
genotype-phenotype correlations: P0111, P0778,<br />
P1209<br />
Genotype-response to drug relation: C56<br />
genotypes: P1204<br />
genotyping: P1137<br />
gentamicin: C58<br />
germline mutation: P0602<br />
germline-methylation: P0760<br />
Gestational hypertensive disorders: P0980<br />
GFAP: P0901<br />
GGCX: P0846<br />
GGN repeats: P0904<br />
GH: P07<strong>16</strong><br />
Gilbert’s syndrome: P0746, P0756<br />
GIS: P1<strong>16</strong>2<br />
Gitelman Syndrome: P1<strong>16</strong>7<br />
GJB1: P0681, P0931<br />
GJB1or Cx32: P0757<br />
GJB2: P0085, P0086, P0754, P0981, P1<strong>16</strong>8, P1171<br />
GLA: P1404<br />
Glaucoma: P0125<br />
glial brain tumors: P0585<br />
Glial tumors: P0555<br />
glioma: P0490, P0556<br />
Globin genes: P1273<br />
Glu298Asp polymorphism: P0982<br />
glucocerebrosidase: P0983<br />
Glucokinase: P0126, P1029<br />
glucose intolerance: P1113<br />
glucose metabolism: P1329<br />
Glutamate receptor: P0974<br />
glutathione S-transferase: P1<strong>16</strong>9<br />
glycolipids: P0725<br />
GM1-gangliosidosis: P0747<br />
Goldenhar: P0210, P1<strong>19</strong>9<br />
Goltz syndrome: P0112<br />
Gomez-Lopez-Hernandez-Syndrome: P0127<br />
gonadal development: P1294<br />
gonadal dysgenesis: P0751<br />
gonadal failure: P0203<br />
Gorlin syndrome: P0128, P0748, P1082<br />
Governance: P1309<br />
GPCR: P1260<br />
GPIIb-IIIa: P0749<br />
Greece: P1206<br />
Grey Zone Alleles: P0114<br />
Grm1: P0750<br />
growth hormone: P1412<br />
Growth hormone receptor: P0984<br />
growth plate: P0693<br />
GST genes polymorphisms: P0849<br />
GST-P1 gene: P0595<br />
gtPBREM: P0746<br />
Guidelines: P1379<br />
gynecological cancers: P0557<br />
H disease: P0429<br />
H1069Q: P0886<br />
H<strong>19</strong>: P0866<br />
HAE: P0991<br />
haematological parameters: P1125<br />
Haematopoietic progenitors: P0205<br />
haemochromatosis: P1350<br />
haemolytic anaemia: P0637<br />
haemophilia: P0129, P0985, P1351<br />
Haplogroup: P0659, P0797, P1135<br />
haplogroups: P1063<br />
haplogroups Y chromosome: P10<strong>16</strong><br />
haploinsufficiency: P0135, P0751<br />
haplotype: P0551, P0962, P0986, P0987, P0998,<br />
P1014<br />
haplotype analysis: P0506<br />
HAPMAP Project: P1236<br />
Harboyan syndrome: P0752<br />
HAX-1: P0753<br />
HAX1 gene mutation: P0062<br />
Hb Valletta: P1170<br />
HB9 protein: P0073<br />
HbA2, MCV, MCH: P1136<br />
HBB: P1098<br />
HbFMalta-I: P1170<br />
HCM: P0130<br />
HCV: P1140<br />
hdac: C66<br />
HDGC: C53<br />
HDL cholesterol: P1153<br />
head growth: P0<strong>16</strong>6<br />
Health care professional training course: P1352<br />
health perception: P1353<br />
healthcare: P1354<br />
Health-e-Child: P0755<br />
heamoglobinopathies: P1315<br />
hearing impairment: P1027<br />
hearing loss: P0117, P0131, P0132, P0244, P0264,<br />
P0754, P1171, P1261, P1355<br />
Heart defect: P0253<br />
Heart development: P0680<br />
heart disease: C82, P0755<br />
Heart failure: P0863<br />
HED,: P0133<br />
Height: P0988<br />
HEK 293: P0543<br />
Helicase: P1114<br />
Helicobacter pylori: P0578<br />
Helicobacter pylori infection: P0359<br />
hematological malignancies: P0546
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