2009 Vienna - European Society of Human Genetics

Keyword Index
Polymalformations: P03.086
polymicrogyria, autosomal recessive,:
P02.112
polymicrogyria: P02.098
polymorphic ventricular tachycardia:
P12.144
polymorphism R577X: P01.01
polymorphism: P04.13, P04.19, P04.28,
P04.30, P05.31, P06.011, P06.029,
P06.041, P06.042, P06.055, P06.067,
P06.088, P06.129, P06.178, P08.39,
P08.56, P08.61, P09.003, P09.088,
P09.102, P09.118, P09.124, P10.15,
P10.18, P10.19, P10.57, P17.24, P17.40
polymorphisms: P02.010, P03.020,
P04.05, P06.039, P06.070, P06.094,
P06.134, P06.143, P08.14, P09.011,
P09.079, P12.062
polyposis coli: P06.153
polyposis: P09.038, P12.129
POMGnT1: P05.41
PON1: P10.13
pontocerebellar hypoplasia: C03.5
Pooling: C01.5
population carrier screening: C18.4
population differentiation: P08.19
population genetics: P10.70, P10.76
population of Lithuania: P09.026
population screening: P01.17, P06.148
population study: P10.88
population: P09.006
Population-based longitudinal study:
P10.79
PORCN gene: P02.038
PORCN: P12.063
Porencephaly: P12.131
Portuguese: P06.122
position effect: P11.020
positional effect: P03.096
position-effect variegation: P03.143
POU3F4: P12.076
power performance: P09.015, P09.129
powerlifting: P09.022
PPAC: P02.105
PPARG: P11.095
PPAR-α: P17.44
PQBP1: P02.199
Prader Willi syndrome: P03.172
Prader Willi/Angelman Syndrome: P01.39
Prader Willi: P03.171, P14.16
Prader-Willi syndrome: P03.175
Prader–Willi/Angelman syndromes:
P03.173
Prader-Willi: P03.174
pre- and protomutations: P16.53
Preaxial Polydactyly: P11.096
preclinical diagnostics: P08.52
predictive genetic testing: P08.33
Predictive testing: P01.21, S03.1
predictive value: P06.014
Preeclampsia: P04.18, P04.19, P05.08,
P05.18, P05.19, P11.097
pregnant: P04.31
Preimplantation genetic diagnosis:
P03.132, P04.15, P05.50, P05.52
Preimplantation: S09.3
premarital screening program: P01.40
premature aging: P02.023
premature centromere separation: P02.102
Premature ovarian failure: C11.4, P04.20,
P04.21, P04.22, P09.099
premature: P02.027
pre-mRNA processing: S02.3
Premutation: P03.153
Prenatal biochemical screening: P05.25
Prenatal diagnosis: P01.41, P02.120,
P02.121, P02.175, P03.046, P05.06,
P05.12, P05.13, P05.26, P05.27, P05.32,
P05.36, P05.43, P05.56, P05.60, P08.58,
P10.25, P16.33, S09.2
prenatal diagnostics: P04.23, P05.28
prenatal evaluation: P05.29
prenatal screening policy: C07.6
prenatal screening: P05.35
prenatal: C07.5, P01.11, P03.113, P05.53,
S09.3
Prenental: P02.172
Prestige oil spill: P03.026
pre-synaptic protein Piccolo: C05.2
prevalence: P02.163
prevention: P14.02
preventive thyroidectomy.: P06.061
Primary arrhythmia syndrome: C13.2
primary care: P01.23
primary cilia: P02.086
Primary ciliary dyskinesia: C12.6
Primary congenital lymphoedema: P12.132
primary cutaneous amyloidosis: P08.53
Primary hypertrophic osteoarthropathy:
P02.157
primitive neuroectodermal tumor: P06.071
Primordial dwarfism: P02.001
professional athletes: P10.69
Progesterone Receptor gene: P06.135
prognosis: P09.082
prognostic: P06.204
prognostically important chromosomal
aberrations: P06.166
promoter function: P11.103
promoter polymorphism: P10.82
Promoter: P02.198, P12.094
properdin: P09.005
prophylactic laparoscopic gastrectomy:
P06.045
prophylaxis: C18.3
propionic acidemia: P12.133
Prostaglandin: P02.157
Prostate cancer (PCa): P06.077
Prostate cancer: P06.028, P06.029,
P06.072, P06.073, P06.074, P06.075,
P06.076, P06.087
protamine gene: P04.30
Protein: P11.098
Protein–Protein interaction: P11.093
protein-protein interaction: P12.134
protein-protein-interaction: C04.4
Proteus syndrome: P12.135
protrombin: P14.17
proximal 3q deletion: P03.076
proximal 6q deletion: P03.077
proximal deletion 3p: P03.073
PSEN1: P12.014
PSEN2: P12.014
pseudomosaicism: P03.047
Pseudoxanthoma elasticum: P12.136
psoriasis: P10.46
Psoriatic arthritis: P09.100, P09.101,
P09.102
PTCH: P06.007
PTEN gene: P06.028, P12.135
PTEN: P06.048, P06.078
PTHR1 gene: P02.158
PTPN11 gene: P02.135
PTPN11: P02.133, P02.141, P02.142,
P02.143, P02.146, P02.147
PTPN22 gene: P09.104, P09.105
PTPN22: P08.54, P09.103, P11.099,
P17.02
public attitude: P01.42
Public Engagement: P01.43
public health: P01.44
public opinion: P01.02
pulmonary arterial hypertension: P17.37
pulse wave analysis: P08.10
purples of Schamberg: P02.113
purples of Shenlejna-Genoh: P02.113
P-value combination: P17.28
Pycnodysostosis: P02.159
pyramidal tetraparesis: P14.04
Q
QF PCR: P05.58, P12.158
QF-PCR: P02.002, P05.55, P05.59,
P05.60, P05.61
QF-PCR;: P03.055
QMPSF: P03.175
qPCR: P11.019, P11.100
qPCR-HRM: P06.079