2008 Barcelona - European Society of Human Genetics

Keyword Index
Gastric cancer: P04.132, P04.146
gastrointestinal cancer: P04.180
Gastroschisis: P01.289, P07.055
GATA4: P06.111
Gaucher: P10.12
GBA: P10.12
G-banding cytogenetics: P02.186
G-banding: P03.30, P07.026
GDAP1 gene: P01.235
GDAP1: P01.227, P01.234
GDF5: P01.130
GEFS+: P05.176
gender: P04.119
gene apolipoproteid A5 polymorphism:
P06.112
Gene carriers: EP14.10
gene conversion: P04.026
Gene copy number variation: S01.2
gene dosage alteration: P06.245
gene dosage imbalance: C05.4
gene expression: C13.5, P02.200, P04.080,
P04.124, P04.125, P04.147, P04.187,
P05.101, P05.137, P05.169, P05.193,
P08.12, P08.16, P08.32, P08.33, P08.49
gene networks: S12.3
gene polimorphism: P06.048
gene polymorphism: P06.007, P06.047,
P06.252
gene polymorphisms: P06.148
gene pool: P07.136
gene prioritisation: C04.5
Gene Regulation: P08.34
gene: P06.098, P09.23
Genealogical tree: EP10.19
gene-disease association: P07.087
gene-environment interaction: P07.012
gene-phenotype correlations: P06.144
genes modifiers of clinical features: P01.033
Genetic algorithms: P08.05
genetic alterations: P04.127
Genetic Biomarkers: S03.4
genetic cancer: EP10.21
genetic counseling: EP01.01, EP10.06,
EP10.19, P01.192, P01.203, P02.168,
P02.196, P09.24
genetic counselling / consultation: EP10.14
Genetic counselling and testing: EPL3.5
genetic counselling protocol: EP10.20
genetic counselling: EP01.09, EP05.1,
EP06.1, EP10.03, EP10.04, EP10.05,
EP10.11, EP10.12, EP10.13, EP10.22,
EP14.07, EPL1.2, EPL2.4, EPL4.4, EW1.1,
EW4.1, P01.021, P01.218, P01.263, P01.267,
P02.129, P05.080, P05.091, P09.25, P09.26,
P09.27, P09.37, P09.56, P09.60, P09.67
genetic counselor: P04.193
genetic determination: P01.264
genetic differentiation: P07.078
genetic disease: P09.28
genetic disorders: P01.001
Genetic diversity: P07.056
genetic education: P09.29
genetic epidemilogy: P06.015
genetic epidemiological study: P01.002
genetic epidemiology: P07.118
genetic epidemyology of hereditary disorders:
P07.057
Genetic health professionals: EP10.10
genetic information: EP10.07, EP10.15,
P09.30, P09.49
Genetic isolate: P06.227
genetic load: P09.52
genetic nurse: EP14.11, EP14.12
Genetic polymorphism: P01.032, P04.126,
P05.104, P06.113, P07.058, P07.097
genetic polymorphisms, SNPs: P06.293
genetic predisposition to common disease:
EPL5.2
Genetic Risk: EP11.2, EPL2.2, S05.3
genetic screening: EPL5.4
genetic service: P09.12
genetic services in Colombia: EP10.14
genetic services: EW2.1, S03.3
genetic syndrome: P01.260
genetic test evaluation: P09.31
genetic test: P09.73
genetic testing of children: EPL2.4
genetic testing: EP07.4, EPL2.1, EPL5.2,
EW2.1, P04.036, P06.253, P09.16, P09.25,
P09.32, P09.33, P09.34, P09.35, P09.40,
P09.61, P09.62
Genetic Therapy: C15.4, S02.1
Genetic variants: P06.158
genetic: EP10.17
genetical genomics: S12.1
genetics education: EP10.07
Genetics Services: EP10.02
genetics: P01.205, P04.008, P06.261,
P09.11, S04.1
genetiko -demographic parameters: P07.059
genic differentiation: P06.155
genogram: EW4.1
Genome instability: P06.114
genome scan: C13.1
genome wide association: C08.5, P06.126,
P06.227
genome wide scan: P06.194, P06.283
genome-wide association scan: P06.115
genome-wide association: C08.6, P07.060,
PL3.2
genome-wide heterozygosity: P07.061
genome-wide linkage: P06.116, P06.208
genome-wide scan: P06.033
genome-wide: P07.068
genomic instability: P02.185
Genomics: P08.59
genotoxicity: P02.185
genotype/phenotype correlation: P01.271
genotype: P06.204, P08.20
genotype-environment interaction: P06.083
genotype-phenotype correlation: P01.066,
P01.117, P01.129, P01.348, P06.067
genotype–phenotype correlation: P01.266
Genotype-phenotype correlations: C06.6
genotype-phenotype: C11.2
genotyping: P01.039, P05.031, P07.069
germline mutations: P04.028
geroderma osteodysplasticum: P06.117
giant cell tumor of bone: P04.147
GJB1 gene: P01.231
GJB2 gene: P01.276
GJB2 mutations: P05.070
GJB2: P05.055, P05.072, P05.073, P06.080,
P07.037
GLA gene: P07.062
GLA: P01.056
glaucoma: P01.290, P01.361, P05.056,
P05.057
GLI1: P04.150
GLI2: P01.155
GLI3: C11.1
glioblastoma multiforme: P04.130
Glioblastoma: P04.148, P04.149
Globin gene regulation: C08.4
globin gene: P01.013
globin: P10.15
glucocorticoid receptor gene: P01.278,
P06.039
glucocorticoid-remediable aldosteronism:
P05.058
Glutamate: P06.235
Glutaryl-CoA dehydrogenase: S11.3
glycogen storage disease type III (GSDIII):
P01.041
Glycosylation: C07.1
GNAS: P05.163
GNE: P05.087
Goldberg-Shprintzen Megacolon syndrome:
P01.133
goldenhar: P01.270
gonadal dysgenesis: P02.105
gonadal mosaicism: P02.150
Gorlin Syndrome: P04.150, P06.118
gout and hyperuricemia: C08.6
gout: P06.303
gr/gr: P02.219
Graves‘ disease: P06.119
Greig syndrome: P01.141
Griscelli Syndrome: P06.120
Grm1: P05.059
growth factors: P05.106
GS-FLX: P08.35
GSK3beta: P06.121
GST polymorphism: P02.241
GST: P06.289
GSTM 1 polymorphism: P04.151
GSTM1 , GSTT1: P04.185
GSTM1: P06.122
GST-P1 polymorphism: P07.063
GSTT1: P06.122
GTF2IRD2: P05.060
guideline: P09.73
guidelines: P01.286, P04.048, P09.25, S05.1
Guinea-Bisssau: P07.050
GVHD: P10.13
GWAS: S06.2
H. pylori: P04.145
habitual abortion.: P02.195
Habitual abortion: P05.061
Haemochromatosis: P07.064, P09.36
Haemoglobin: P01.020, P07.124