2009 Vienna - European Society of Human Genetics

Keyword Index
haplotype sharing analysis: C13.1
haplotype: P06.030, P12.029
Hardware: P15.05
Hardy-Weinberg: P10.55
Hb A2 NYU: P12.073
Hb variant: P12.074
HBA1, HBA2: P02.170
HbA1c: P17.03
HbD: P12.001
HbF: P12.002
HBOC: P06.040
HCC: P06.041, P06.042
HCM: P16.22
HCV: P11.053
H-disease: P02.178
Headache: P09.049
Health Care Needs Assessment: P01.32
Health professionals: P01.29
Hearing impairment: C14.3, P12.075,
P12.076
Hearing loss: P02.043, P11.032, P12.077
HEARING LOSSES: P12.046
heart defects: P02.017
Heart Development: C11.2, C12.1,
P11.015
Heart Failure: P16.12
heart malformation: P02.005
Heart Transplant: P16.12
heart: P06.070, P09.013
height: P08.49, S06.2
HELLP syndrome: P05.14, P05.15
Hemangioma: P02.092
Hematological: C17.3
hematopoietic stem cells: S12.2
hemiatrophy: P03.108
hemochromatosis: P02.044
Hemodialysis: P03.042
hemoglobine S: P02.109
hemoglobinopathies: P12.074, P12.078
Hemoglobinopathy: P01.40
hemophilia A: P11.052, P12.079
Hemophilia B: P12.080, P14.10
hepatic lipoprotein metabolism: P09.003
Hepatitis: P11.053
hepatocellular carcinoma: P06.043,
P06.088
hepcidin: P12.094
HER2/neu: P06.136
Hereditary breast and ovarian cancer:
P06.120
Hereditary breast cancer: P06.121,
P06.130
Hereditary breast-ovarian cancer: P06.131
Hereditary Diffuse Gastric Cancer:
P06.044
hereditary disorders: P02.045, P11.046
HEREDITARY FOLATE
MALABSORPTION: P13.24
hereditary gastric cancer: P06.045
Hereditary hearing loss: P08.34
hereditary hemochromatosis: P02.181,
P13.25
Hereditary multiple exostoses: P02.046,
P13.26
Hereditary Nervous System Diseases:
P10.37
Hereditary Nonpolyposis Colorectal Cancer
(HNPCC): P06.149
Hereditary nonpolyposis colorectal cancer:
P06.146
hereditary optic atrophy: P12.082
hereditary pathology: P03.109
hereditary predisposition: P06.125
Hereditary Sclerosing Poikiloderma of
Weary: P09.050
Hereditary Spastic Paraplegia (HSP):
P12.083, P12.084, P12.085
herg: P06.174
heritability: P10.85
heroin dependence: P09.051
heterogeneity: P08.35, P12.086, P12.107
heterogeneous phenotype: P03.088
heterogenous disorders: P11.054
heteroplasmy: P05.39, P11.075
HFE gene: P09.078
HFE: P02.044, P12.072, P13.25, P17.52
HGO mutations: P12.009
HGSNAT: P13.41
high resolution melting: P03.150, P06.132,
P09.058, P11.055, P15.07
high throughput: P11.092
high-resolution melting analysis: P10.62,
P11.056
High-throughput Real-Time PCR: P10.79
high-throuput sequencing: C01.3
hip dislocation: P03.107
Hirschsprung’s disease: C17.4, P03.148,
P09.052, P10.38
Histomorphometry: C08.2
historical relics: C09.5
HL-60: P06.175
HLA Class I Diversity: P10.39
HLA Class II Diversity: P10.39
HLA polymorphisms: P10.40
HLA: C09.1, P10.31, P11.101
HLA-B27: P03.028
HLA-C: P09.101
HLA-DRB1 alleles: P08.57
HMGA2: P03.072
HMGCS2: P11.057
HNPCC testing: P06.157
HNPCC: P01.03, P06.147, P06.148,
P06.150, P06.152, S13.2
HNPP: P12.086
holoprosencephaly: P02.047, P02.048,
P02.089, P03.029, P12.147
Holt-Oram syndrome: P02.049
homer1: P17.54
homocysteine: P17.27
homocysteinemia: P13.47
homogenization: P11.007
Homologous recombination: P14.11
homozygosity mapping: P08.55
homozygosity: P08.07, P10.41
homozyosity mapping: P16.04
hormonal control: P17.07
hotspot: P12.025
HOXD cluster: P03.030
HPGD: P02.157
HPLC: P12.158
HPRT1: P12.104
HPV infection: P07.05
HPV: P06.046, P11.058
H-ras: P06.039
HRM: P11.059, P11.060, P12.021
HS-111: P12.002
HSP: P02.202
HSPC300: P06.100
hTERC: P06.181
hTERT: P06.175
HTR3: P09.007
HTR3C: P09.063
HTRA2: P17.55
Human cancer: S12.1
Human coagulation factor IX: P14.10
human cognitive abilities: P08.32
Human genotoxicity: P03.024
human inherited disease: C15.3
human lymphocytes: P03.041
human meiotic recombination: C09.3
Human metaphase chromosomes:
P03.024
human myocardial infarction: P17.33
human papillomavirus detection: P06.026
human papillomavirus: P06.026
human skin fibroblasts: P11.036
human variation: C09.2
Human: P02.099, P10.42
Hungarian: P10.46
Hungary: P02.125
huntingtin: P10.43
huntington disease gene: P10.43
Huntington disease like 2: P12.089
Huntington disease: P01.33
Huntington Horea: P12.090
Huntington: P12.087, P12.088
Huntington’s disease: P12.091, P12.092
hydranencephaly-hydrocephaly: P02.050