2009 Vienna - European Society of Human Genetics

Keyword Index
P11.013, P11.014, P11.071, S12.3
candidate gene: P16.02
Candidate genes: P08.20, P09.125
canine melanocortin-4 receptor gene:
P09.023
cannabis: P10.19
Canton Sarajevo residents: P10.88
Capability: P01.23
capillary electrophoresis: P02.194, P05.09,
P05.17, P11.077
CAPN3: P16.45, P16.46
capture: P11.035
carbamazepine: P17.65
carcinoma in situ cells: P06.025
Cardiac arrhythmia: P16.15
Cardiac genetics: P16.07
cardiac: C02.2, P16.06
cardiofaciocutaneous syndrome: P02.139
cardiogenetics: P16.16, S03.1
Cardiomyopathy: P16.08, P16.10, P16.17,
P16.28, S03.3
cardiovascular disease: P08.18, P17.26,
P17.44
Cardiovascular malformations: P11.015
cardiovascular: P03.182, P09.091
Cardivascular disease: C17.3
carer: P01.33
caries: P08.67
carotid atherosclerosis: P17.25
carrier status: P01.37
carrier: P10.35
Case Report: P02.102
Case studies: P11.082
case-control association study: P09.110
case-control study: P08.19, P10.04
Cataract: P12.117
CATARACTS: P02.165
Catechol-O-methyltransferase: P10.10
Caudal appendage: P03.106
Caveolin-1: P09.024
CBAVD/CUAVD syndromes: P02.119
cbl: S11.1
cblF: P13.08
CD244: P09.109
CD44: P09.031
CDG type Ia: P12.028
CDH1 Deletions: P06.044
CDH1 MLH1 MSH2: P06.034
CDH1-160 polymorphism: P06.035
CDK5R1: P11.016
CDKL5: P02.183, P02.187, P02.188,
P02.189, P02.192
CDKN1C: P03.149
celiac disease: C09.1, P02.096, P09.025,
P12.029
celiac: C17.5
cell cycle: P05.07, P06.082
cell free DNA: P05.08
cell free fetal DNA: P05.09
cell-free fetal nucleic acids: S09.2
Celtic heritage: P10.89
Centa2 and Suz12: P11.015
Centaurin-alpha2: P11.017
centronuclear myopathy: P16.38
cerebellar ataxia: P12.030
cerebellar atrophy: P02.055
cerebral malformation: P02.047
cerebral palsy: P14.04
cerebral small vessel disease: P17.21
Ceruloplasmin: P17.51
cervical cancer, genes: P07.05
cervical cancer: P11.058
Cervical carcinoma: P06.026
Cervival intraepithelial neoplasia: P06.047
CF: P02.131
CFTR gene mutations: P02.119
CFTR gene: P02.123, P03.198
cftr variants: P02.129
CFTR: P02.117, P02.120, P02.122,
P02.124, P02.131, P03.191, P11.018,
P11.050, P15.03
CGD: P12.031
CGG repeats: P03.154
CGH: P03.166, P12.026
CGH-array: P03.089, P06.112, P06.159
CHAPERONE: P12.067
Charcot-Marie-Tooth disease: P16.33
Charcot-Marie-Tooth: P16.35
CHARGE syndrome: P02.017
CHD7: P02.017
cheilognathopalatoschisis: P05.29
CHEK2 mutations: P06.114
CHEK2: P06.124
chemotherapy: P06.141
Chernobyl NPP: P07.02
Cherubism: P02.018
CHIARI I: P12.032
child: P02.015, P02.149
Childhood acute lymphoblastic leukemia:
C06.6
childhood BCP-ALL: P06.199
childhood: P16.23
Children: P01.16, P03.033, P05.44,
P05.49, P06.169, P08.16
Chimeric antigen receptor: P06.091
chimerism: P11.019
Chinese: P12.044
CHM: P12.034
Choice of spouse: P10.09
cholesterol: P13.20
chondrodysplasia: P12.033
Choroideremia: P12.034
Chr 7 and 8: P06.190
CHRNA7: C02.3, P03.174
chromium: P03.013
chromosomal aberrations: P03.014,
P03.053, P03.109, P04.25
Chromosomal Abnormalities: C18.5,
P02.074, P03.034, P03.122, P06.184,
P06.185
Chromosomal alterations: P03.009,
P03.039, P03.044
chromosomal anomaly: C07.6, P03.098
chromosomal deletion: P03.129
chromosomal diseases: P05.28
chromosomal mosaicism: P03.054
chromosomal rearrangement: P03.008
chromosomal studies: P03.031
chromosomal translocation: P03.119
chromosomally unbalanced sperm: P04.08
chromosome 10: P03.121
chromosome 15: P08.59
chromosome 18: P03.090
chromosome 2p: P03.036
chromosome 4: P02.005
chromosome 6: P03.162
chromosome 8: P07.04
chromosome 9: P08.46
Chromosome aberations: P03.015
chromosome aberrations: C11.1
chromosome abnormalities: P04.06
chromosome alterations: P03.026
Chromosome instability: P03.004, P03.135
Chromosome organization: P03.006
chromosome study: P06.186
chromosome territory: C16.1
chromosome Y: P03.189
chromosome: C16.4, P03.010, P06.103,
P12.041
chromosomes: P03.169
chromosomopathies: P03.120
Chromsome 17q24: P03.091
chronic cervicitis: P06.022
chronic granulomatous disease: P12.114
chronic heart failure: P17.30
chronic lymphocytic leukaemia: P06.202
chronic lymphocytic leukemia: P06.170,
P06.187
chronic myeloid leukemia Ph1+: P06.191
chronic myeloid leukemia: P06.188,
P06.189, P06.190, P06.201
chronic pancreatitis: P12.035
chrosomal aberration of fetus: P05.24
Chuvashiya: P10.44
ciliary disorders: P12.036
ciliopathy: C03.2, P02.019
cirrhosis: P12.004
cis acting elements: P08.11