Gene: HTC2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3342
Gene Symbol: HTC2
HTC2 		0.050 Biomarker disease BEFREE The combined use of MLPA and array CGH is an effective and specific means to diagnose WHS and allows for the precise identification of the breakpoints and sizes of deletions. 26960370 2016
Entrez Id: 3342
Gene Symbol: HTC2
HTC2 		0.050 Biomarker disease BEFREE Three unusual 4p16.3 deletions were detected by array-CGH in absence of a obvious clinical diagnosis of WHS. 24738919 2014
Entrez Id: 3342
Gene Symbol: HTC2
HTC2 		0.050 Biomarker disease BEFREE Comprehensive analysis of Wolf-Hirschhorn syndrome using array CGH indicates a high prevalence of translocations. 17726485 2008
Entrez Id: 3342
Gene Symbol: HTC2
HTC2 		0.050 Biomarker disease BEFREE High-resolution karyotype and microarray-CGH using an oligonucleotide array with 75Kb oligo's were normal, excluding Wolf-Hirschhorn syndrome. 17140870 2007
Entrez Id: 3342
Gene Symbol: HTC2
HTC2 		0.050 Biomarker disease BEFREE Both FISH and microarray CGH studies clearly demonstrated that the WHS critical regions 1 and 2 were deleted, and that the BWS imprinted domains (ID) 1 and 2 were duplicated on the der(4). 17603794 2007