2009 Vienna - European Society of Human Genetics

Keyword Index
gene networks: S12.2
gene of angiotensin-converting enzyme
ACE: P17.15
gene polymorphism: P04.04
gene polymorphisms: P06.010
gene scanning: P11.056
gene structure: P11.044
gene terapy: P12.103
gene testing: P01.18
gene therapy: C12.3, C12.6, P14.14
gene variants: P09.047
gene*medication interaction: P09.108
gene: P02.077, P04.19, P04.28, P12.077,
P16.08
GENE1: P08.31
genealogies: P10.50
GeneChip resequencing array: P11.045
gene-expression: P12.106
Generalized Atrophic Benign Epidermolysis
Bullosa: P12.068
genes GSTT1 and GSTM1: P10.27
Genes of interleukins: P10.28
genethics: P01.15
Genetic Analysis: P15.05, P17.59
genetic and epigenetic: P09.117
Genetic association study: P06.066
genetic association: C05.2, P09.100
Genetic counseling: P01.20, P01.38,
P01.40
genetic counselling: C18.6, P01.21,
P02.181, P03.005, P03.135, S03.2
genetic damage.: P03.044
Genetic diagnosis: P10.23, P11.038,
P12.016
Genetic diagnostic: P16.27
genetic diagnostics: P11.101
genetic disease: P01.22
Genetic Diseases: P02.070
Genetic distances matrices: P10.30
genetic diversity of genes: P11.046
Genetic diversity: P10.29
genetic education: P01.23
Genetic epidemiology: P10.34, P11.046,
PL1.1
Genetic heterogeneity: P08.46, P12.036
genetic identification: C09.5
genetic information: P01.24
genetic isolates: C09.6
Genetic load: P09.126
Genetic Mapping: P08.47
genetic markers from GWAS: P09.056
genetic mutation: P02.116
Genetic mutations: P13.14
Genetic nurses and counsellors: P01.25
genetic polymorphism: P08.23
genetic profile: P06.068
Genetic profiles: P10.07
Genetic research: P01.26
genetic results: C18.1
genetic risk factor: P09.010, P10.04
genetic risk factors: P06.049
genetic screening: P01.27, P03.022
genetic services: P01.04, P02.118
Genetic susceptibility: P09.073, P17.69
Genetic testing and research: P01.29
Genetic testing: P01.16, P01.28, P02.007,
P06.105, P11.037, P15.13
genetic variability: P10.30
genetic variation: P09.040
Genetic: P01.19, P01.39
genetical etiology: P02.028
genetic-epigenetic: P03.173
genetics education: P01.31
genetics polymorphism: P17.35
genetics: C17.1, P01.30, P08.65, P12.168,
P15.09
Genital Human Papillomavirus: P06.047
genodermatology: P02.042
genome analysis: P11.025
genome wide analysis: P09.048
Genome Wide Association Study: P08.51,
P09.032
genome wide association: C05.6, P17.27
Genome: P11.110
Genome-wide association analysis: C10.2
genome-wide association scan: C17.6,
P08.13
genome-wide association studies: C10.6,
P10.32, PL2.1,S06.2, S13.1
genome-wide association: P10.31
Genome-wide expression analysis: C10.2
Genome-wide linkage scan: P08.32
genomic deletion: S08.2
Genomic Imprinting: C08.6
genomic medicine: P08.33
genomic selection: C01.3
Genomics of Lipid-associated Disorders:
PL1.1
genomics: P10.33
Genotoxicity: P03.025, P03.026
genotype: P06.006, P08.22, P11.047,
P11.048, P11.065
genotype-phenotype correlation: P02.053
Genotype-Phenotype: C15.5, P12.120
genotyping: P06.020, P11.055
Geographical endogamy: P10.09
Georgia: P10.24
Germline mutation: P06.146
Germline: P06.044
Gestational Diabetes Mellitus (GDM):
P05.56
GGC repeats: P03.188
GIGYF2: P17.61
Gilbert syndrome: P11.049
Gitelman syndrome: P12.138
GJB1: P16.34, P16.36
GJB2: P10.34, P10.35, P10.65, P12.046,
P12.053, P12.069, P12.123
GJB6: P12.053
GLA gene: P13.13
GLA: P13.12
glaucoma: P12.070
Gleevec: P06.191
GLI3: C04.4
glucocerebrosidase: P13.42
glucocorticoid receptor gene: P08.16
glucocorticosteroids: P02.010
glucokinase polymorphism: P17.43
glucose: P17.04
GLUT1: P13.21
Glutathione peroxidase 1: P09.095
glutathione-S-transferase P1 gene:
P06.075
glyccogen-branching enzyme: P13.23
glycerol kinase deficiency: P13.22
Glycogen storage disease: P13.23
glycogen synthase kinase: P09.068
glycogen-debranching enzyme: P13.23
Golgi apparatus: C08.4
Goltz syndrome: P12.063
gonadal mosaicism: P03.067
governance: P01.13
Graves’ disease: P08.54
GRIA3: P02.195
Gross deletion: P12.072
growth delay: P03.127
growth retardation: P03.134
growth: P03.072
GS-FLX: P11.050
GSTT1,M1,P1: P06.142
GTG-banding: P03.027
GTP-6 cyclohydrolase (GTPC) deficiency:
P13.06
Guidelines: P01.10
GUSB gene defect: P05.21
GWAS: C10.3, C10.4, C13.6, C17.1,
P09.055, P09.062, P10.03, P10.36,
P11.051, P17.28
H
H DISEASE: P12.071
H19: C08.5
Haemochromatosis: P12.072, P14.19
hair abnormalities: P02.052
HAND1: P12.043
haplogroups: P10.58
haploinsufficiency: P16.26
haplotype analysis: P08.53, P08.64