2008 Barcelona - European Society of Human Genetics

Keyword Index
venous thrombosis: P06.319
ventriculomegaly: P03.71
vera: P01.318
vesico-ureteric reflux: P06.312
VHL gene: P04.207
VHL: P05.132
violence: EP14.23
viruses: P09.67
vision: C12.4
Vitamin A deficiency: P01.342
vitamin A: P01.046
vitamin D deficient rickets: P06.313
Vitamin D: P07.086
Vitamin K: P08.84
vitamins: P10.22
VKORC1: P07.130, P08.82
VLDLR: C07.5, P01.353
VLGR1: P06.314
volunteers: P09.59
von Hippel Lindau syndrome (VHL): EP13.8
Von Hippel-Lindau: P04.207
VWD: P05.206
VWF gene: P05.206
W748S POLG mutation: P01.345
Waardenburg-Shah: P02.087
Warfarin dosing: P08.84
warfarin: P08.83
WASP: P05.196
Watson Syndrome: P01.175
Werner syndrome: P01.149
Western Anatolia: P07.025, P07.133
Western blot: P01.225
WFS1: P05.207
WGA: P08.85
White hair: P06.037
White matter abnormalities: P01.060,
P01.133
white matter: P05.100
WHO: S03.2
whole arm translocation: P04.079
whole-arm rearrangement: P04.074
whole-genome amplification: P08.86
Wiki: P08.15
Williams Syndrome: P02.052
Williams-Beuren Syndrome: P05.060
Wilson and Menkes diseases: P01.072
Wilson disease: P01.049, P01.073, P01.074,
P07.131
Wnt pathway: P04.100
Wnt/b-catenin signalling pathway: P04.153
Wnt/beta-catenin: P05.141
Wolf-Hirschhorn syndrome: P02.043,
P02.045, P02.047, P02.048
Wolf-Hirschorn: P02.044
women karyotyping: P02.216
X chromosome imbalance: P01.341
X chromosome: P02.177, P06.035, P07.056,
PL3.1
X inactivation analysis: P04.067
XALD: P01.075
X-ALD: P01.076, P03.57, P10.27
X-autosome translocation: P02.217
X-Chromosome: C07.4, P07.114
xenobiotic-metabolising enzimes: P06.282
xenobiotic-metabolizing genes: P07.132
Xenobiotics: P04.126
xeroderma pigmentousm, Cockayne
syndrome: P05.208
X-fragile Syndrome: P01.116
X-inactivation: P02.217
XIST: P04.053
X-linked congenital motor nystagmus:
P01.369
X-linked dominant: P05.149
X-linked hypohidrotic ectodermal dysplasia:
P05.209
X-linked inheritance: EP10.24
X-linked juvenile Retinoschisis: P05.210
X-linked mental retardation (XLMR): P06.315
X-linked mental retardation: P01.082,
P01.084, P01.087, P01.109
X-linked ocular albinism type 1: P06.324
X-linked : P01.102
X-linked: EP03.1, EP10.23, EPL6.1,
P01.228, P06.059
XLMR: C01.2, C07.6, P01.099, P01.103,
P01.110, P02.061, P02.062
XLRS: P05.210
XmnI polymorphism: P01.014
Xp deletion: P01.089
XPB: P05.208
Xq duplication: P01.085
Xq28: C06.1
XRCC1: P07.133
X-skewing: C10.6
XX male: P02.103
XXY: EP14.14
xy sex reversal: P02.104
XYY: P02.218
Y chromosome abnormalities: P02.221
Y chromosome, microdeletion: P09.63
Y chromosome: P02.220, P05.211, P06.006,
P07.056, P07.110, P07.134, P07.135
Y haplogroups: P05.211
Y microdeletion: P02.219, P02.235, P02.240
Y mosaicism: P02.085
Yakut populations: P07.121
Y-chromosomal: P07.113
Y-chromosome microdeletion: P06.316
Y-chromosome SNP´s: P07.084
y-chromosome SNPs: P07.137
Y-chromosome: P07.129, P07.136
Y-chromosomes lineages: P07.138
yeast two hybrid: P05.157
yeast: P05.008, S09.3
young maternal age: P07.055
Yq Microdeletion: P01.370
YSTR-haplotypes: P07.136
ZEB2: P01.326
Zellweger spectrum: S11.1
ZFHX1B: P01.325
ZFX haplotypes: P07.078
ZFYVE27: P05.212
ZMPSTE24: P03.72
ZNF750: P06.317
ZRS: P01.149, P01.167, P01.169