LEADER 03439oas 2201261 a 450 001 9910144004103321 005 20251105213014.0 011 $a1098-1004 035 $a(DE-599)ZDB1498165-8 035 $a(DE-599)1498165-8 035 $a(OCoLC)38849524 035 $a(CONSER)sn 98009192 035 $a(CKB)954925597586 035 $a(EXLCZ)99954925597586 100 $a19980326a19929999 sy a 101 0 $aeng 135 $aurcnu|||||||| 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 10$aHuman mutation 210 $a[New York, N.Y.] $cWiley-Liss, Inc.$d1992- 210 2 $a[London, United Kingdom] $cHindawi Limited ;$a[Hoboken, NJ] $cWiley Periodicals, Inc 210 3 $a[Hoboken, NJ] $cWiley Periodicals, Inc 300 $aRefereed/Peer-reviewed 311 08$a1059-7794 531 0 $aHuman mutat. 606 $aHuman chromosome abnormalities$vPeriodicals 606 $aMutation (Biology)$vPeriodicals 606 $aMedical genetics$vPeriodicals 606 $aMedical genetics 606 $aMutation$xgenetics 606 $aGenetics, Medical 606 $aGe?ne?tique me?dicale$xPe?riodiques 606 $aChromosomes humains$xAnomalies$vPe?riodiques 606 $aMutation (Biologie)$vPe?riodiques 606 $aGe?ne?tique me?dicale 606 $aMedical genetics$2fast$3(OCoLC)fst01014133 606 $aHuman chromosome abnormalities$2fast$3(OCoLC)fst00962907 606 $aMutation (Biology)$2fast$3(OCoLC)fst01031152 606 $aCromosomes humans$2thub 606 $aMutació (Biologia)$2thub 606 $aGenètica mèdica$2thub 608 $aperiodicals.$2aat 608 $aPeriodicals.$2fast 608 $aPeriodicals.$2lcgft 608 $aPe?riodiques.$2rvmgf 608 $aRevistes electròniques.$2thub 615 0$aHuman chromosome abnormalities 615 0$aMutation (Biology) 615 0$aMedical genetics 615 0$aMedical genetics. 615 12$aMutation$xgenetics. 615 22$aGenetics, Medical. 615 6$aGe?ne?tique me?dicale$xPe?riodiques. 615 6$aChromosomes humains$xAnomalies 615 6$aMutation (Biologie) 615 6$aGe?ne?tique me?dicale. 615 7$aMedical genetics. 615 7$aHuman chromosome abnormalities. 615 7$aMutation (Biology) 615 7$aCromosomes humans. 615 7$aMutació (Biologia) 615 7$aGenètica mèdica. 676 $a616 712 02$aWiley-Liss Inc., 712 02$aHuman Genome Variation Society, 801 0$bNSD 801 1$bNSD 801 2$bNLM 801 2$bOCLCQ 801 2$bMYG 801 2$bOCLCQ 801 2$bOCL 801 2$bIUL 801 2$bU9S 801 2$bOCLCQ 801 2$bUKMGB 801 2$bOCLCQ 801 2$bMYG 801 2$bOCLCF 801 2$bOCLCQ 801 2$bNLE 801 2$bOCLCQ 801 2$bCGU 801 2$bOCLCQ 801 2$bVT2 801 2$bOCLCO 801 2$bOCLCA 801 2$bOCLCO 801 2$bOCL 801 2$bOCLCQ 801 2$bUAB 801 2$bAUD 801 2$bYWS 801 2$bDLC 801 2$bOCLCL 801 2$bCCO 801 2$bW2U 801 2$bS2H 801 2$bCSU 801 2$bLIP 801 2$bCASUM 801 2$bOCLCQ 906 $aJOURNAL 912 $a9910144004103321 996 $aHuman mutation$9796157 997 $aUNINA