VIAF

Virtual International Authority File

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Leader 00000nz a2200037n 45 0
001 WKP|Q114408026 (VIAF cluster) (Authority/Source Record)
003 WKP
005 20241121000245.0
008 241121nneanz||abbn n and d
035 ‎‡a (WKP)Q114408026‏
035 ‎‡a (OCoLC)Q114408026‏
100 0 ‎‡a Ming-Huei Lin‏ ‎‡c researcher‏ ‎‡9 en‏
670 ‎‡a Author's Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism‏
670 ‎‡a Author's Detection of altered methylation status at 11p15.5 and 7q32 in placental mesenchymal dysplasia‏
670 ‎‡a Author's Directly transmitted 4.5-Mb triplication of 4q12-q13.1: prenatal diagnosis and molecular cytogenetic characterization‏
670 ‎‡a Author's Osteogenesis imperfecta type IV: prenatal molecular diagnosis and genetic counseling in a pregnancy carried to full term with favorable outcome‏
670 ‎‡a Author's Partial monosomy 13q (13q21.32--->qter) and partial trisomy 8p (8p1--->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization‏
670 ‎‡a Author's Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT‏
670 ‎‡a Author's Rapid detection of K650E mutation in FGFR3 using uncultured amniocytes in a pregnancy affected with fetal cloverleaf skull, occipital pseudoencephalocele, ventriculomegaly, straight short femurs, and thanatophoric dysplasia type II‏
919 ‎‡a prenataldiagnosisandarraycomparativegenomichybridizationcharacterizationofinterstitialdeletionsof8q233q2411and8q2413associatedwithlangergiedionsyndromecorneliadelangesyndromeandhaploinsufficiencyoftrps1rad21andext‏ ‎‡A Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT‏ ‎‡9 1‏
919 ‎‡a partialmonosomy13q13q2132qterandpartialtrisomy8p8p1pterpresentingwithanencephalyandincreasednuchaltranslucencyarraycomparativegenomichybridizationcharacterization‏ ‎‡A Partial monosomy 13q (13q21.32--->qter) and partial trisomy 8p (8p1--->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization‏ ‎‡9 1‏
919 ‎‡a osteogenesisimperfectatype4prenatalmoleculardiagnosisandgeneticcounselinginapregnancycarriedtofulltermwithfavorableoutcome‏ ‎‡A Osteogenesis imperfecta type IV: prenatal molecular diagnosis and genetic counseling in a pregnancy carried to full term with favorable outcome‏ ‎‡9 1‏
919 ‎‡a directlytransmitted45mbtriplicationof4q12q131prenataldiagnosisandmolecularcytogeneticcharacterization‏ ‎‡A Directly transmitted 4.5-Mb triplication of 4q12-q13.1: prenatal diagnosis and molecular cytogenetic characterization‏ ‎‡9 1‏
919 ‎‡a detectionofalteredmethylationstatusat11p155and7q32inplacentalmesenchymaldysplasia‏ ‎‡A Detection of altered methylation status at 11p15.5 and 7q32 in placental mesenchymal dysplasia‏ ‎‡9 1‏
919 ‎‡a applicationofnoninvasiveprenataltestinginlategestationinapregnancyassociatedwithintrauterinegrowthrestrictionandtrisomy22confinedplacentalmosaicism‏ ‎‡A Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism‏ ‎‡9 1‏
919 ‎‡a rapiddetectionofk650emutationinfgfr3usingunculturedamniocytesinapregnancyaffectedwithfetalcloverleafskulloccipitalpseudoencephaloceleventriculomegalystraightshortfemursandthanatophoricdysplasiatype2‏ ‎‡A Rapid detection of K650E mutation in FGFR3 using uncultured amniocytes in a pregnancy affected with fetal cloverleaf skull, occipital pseudoencephalocele, ventriculomegaly, straight short femurs, and thanatophoric dysplasia type II‏ ‎‡9 1‏
996 ‎‡2 LC|no2019084434‏
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996 ‎‡2 ERRR|12367990‏
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996 ‎‡2 LNB|LNC10-000208394‏
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997 ‎‡a 0 0 lived 0 0‏ ‎‡9 1‏