WHSC1

AcronymDefinition
WHSC1Wolf-Hirschhorn Syndrome Candidate 1
References in periodicals archive ?
LETM1 (OMIM 604407), WHSC1 (OMIM 602952), and FGFR3 (OMIM 134934) were deleted in all patients evaluated by array CGH.{Figure 1}{Figure 2}{Figure 3}{Table 2}
WHSC1 and FGFR3 were deleted in the patients detected by array CGH, and the absence of expression of these two gene has been associated with the typical craniofacial features of WHS, obvious growth delay, and skeletal disorders.
of Locus and Name % Cases Comment * 1p tel 002 1PTEL06 25 2/8 Sub Tel 1q tel 023 1QTEL10 38 3/8 Sub Tel 2p tel 024 U32389 25 2/8 Sub Tel 2p13 [right arrow] p12 028 REL 25 2/8 Amp 2q tel 038 D2S447 25 2/8 Sub Tel 4p16.3 059 WHSC1 25 2/8 5q tel 077 5QTEL70 38 3/8 Sub Tel 11p tel 140 INS 25 2/8 Sub Tel 15q tel 188 WI-5214 25 2/8 Sub Tel 19p tel 237 stSG42796 38 3/8 Sub Tel 20p tel 244 20PTEL18 25 2/8 Sub Tel * Sub Tel indicates sub telomeric sequence; Amp, cancer amplicon previously described in the literature.