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1 Ergebnisse
1
eP390: Leveraging unique chromosomal microarray probes to r..:
Sack, Laura
;
Mertens, Lauren
;
Murphy, Elissa
...
Genetics in Medicine. 24 (2022) 3 - p. S246 , 2022
Link:
https://doi.org/10.1016/j.gim.2022.01.425
RT Journal T1
eP390: Leveraging unique chromosomal microarray probes to resolve complex copy number variation at the highly homologous deafness-infertility syndrome locus at 15q15.3
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.gim.2022.01.425&Exemplar=1&LAN=DE A1 Sack, Laura A1 Mertens, Lauren A1 Murphy, Elissa A1 Hutchinson, Laura A1 Giersch, Anne A1 Mason-Suares, Heather PB Elsevier BV YR 2022 SN 1098-3600 JF Genetics in Medicine VO 24 IS 3 SP S246 LK http://dx.doi.org/https://doi.org/10.1016/j.gim.2022.01.425 DO https://doi.org/10.1016/j.gim.2022.01.425 SF ELIB - SuUB Bremen
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