Search
Leader | 00000nz a2200037n 45 0 | ||
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001 | WKP|Q56424218 (VIAF cluster) (Authority/Source Record) | ||
003 | WKP | ||
005 | 20241020233146.0 | ||
008 | 241020nneanz||abbn n and d | ||
035 | ‡a (WKP)Q56424218 | ||
024 | ‡a 0000-0002-6041-1763 ‡2 orcid | ||
024 | ‡a 56543924200 ‡2 scopus | ||
035 | ‡a (OCoLC)Q56424218 | ||
100 | 0 | ‡a João Silva ‡c researcher ORCID: 0000-0002-6041-1763 ‡9 en | |
375 | ‡a 1 ‡2 iso5218 | ||
400 | 0 | ‡a João Silva ‡c onderzoeker ‡9 nl | |
670 | ‡a Author's CADASIL: MRI may be normal in the fourth decade of life - a case report. | ||
670 | ‡a Author's Complementarity between medical geneticists and genetic counsellors: its added value in genetic services in Europe | ||
670 | ‡a Author's Development of NIPBL locus-specific database using LOVD: from novel mutations to further genotype-phenotype correlations in Cornelia de Lange Syndrome | ||
670 | ‡a Author's Further clinical and molecular delineation of the 15q24 microdeletion syndrome | ||
670 | ‡a Author's [Genetics on Primary Healthcare: A Multidisciplinary Perspective] | ||
670 | ‡a Author's Mutations in genes encoding condensin complex proteins cause microcephaly through decatenation failure at mitosis | ||
670 | ‡a Author's Paternal transmission of subcortical band heterotopia through DCX somatic mosaicism. | ||
670 | ‡a Author's Redefining the MED13L syndrome | ||
670 | ‡a Author's Spectrum of Atypical Clinical Presentations in Patients with Biallelic PRF1 Missense Mutations | ||
670 | ‡a Author's The contribution of 7q33 copy number variations for intellectual disability | ||
909 | ‡a (scopus) 56543924200 ‡9 1 | ||
909 | ‡a (orcid) 0000000260411763 ‡9 1 | ||
919 | ‡a cadasilmrimaybenormalinthe4decadeoflifeacasereport ‡A CADASIL: MRI may be normal in the fourth decade of life - a case report. ‡9 1 | ||
919 | ‡a spectrumofatypicalclinicalpresentationsinpatientswithbiallelicprf1missensemutations ‡A Spectrum of Atypical Clinical Presentations in Patients with Biallelic PRF1 Missense Mutations ‡9 1 | ||
919 | ‡a paternaltransmissionofsubcorticalbandheterotopiathrough610somaticmosaicism ‡A Paternal transmission of subcortical band heterotopia through DCX somatic mosaicism. ‡9 1 | ||
919 | ‡a redefiningthemed13lsyndrome ‡A Redefining the MED13L syndrome ‡9 1 | ||
919 | ‡a contributionof7q33copynumbervariationsforintellectualdisability ‡A The contribution of 7q33 copy number variations for intellectual disability ‡9 1 | ||
919 | ‡a geneticsonprimaryhealthcareamultidisciplinaryperspective ‡A [Genetics on Primary Healthcare: A Multidisciplinary Perspective] ‡9 1 | ||
919 | ‡a mutationsingenesencodingcondensincomplexproteinscausemicrocephalythroughdecatenationfailureatmitosis ‡A Mutations in genes encoding condensin complex proteins cause microcephaly through decatenation failure at mitosis ‡9 1 | ||
919 | ‡a furtherclinicalandmoleculardelineationofthe15q24microdeletionsyndrome ‡A Further clinical and molecular delineation of the 15q24 microdeletion syndrome ‡9 1 | ||
919 | ‡a developmentofnipbllocusspecificdatabaseusinglovdfromnovelmutationstofurthergenotypephenotypecorrelationsincorneliadelangesyndrome ‡A Development of NIPBL locus-specific database using LOVD: from novel mutations to further genotype-phenotype correlations in Cornelia de Lange Syndrome ‡9 1 | ||
919 | ‡a complementaritybetweenmedicalgeneticistsandgeneticcounsellorsitsaddedvalueingeneticservicesineurope ‡A Complementarity between medical geneticists and genetic counsellors: its added value in genetic services in Europe ‡9 1 | ||
946 | ‡a b ‡9 1 | ||
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