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1 Ergebnisse
1
Phänotypische und genotypische Diagnostik bei non-syndromal..:
Rosenfeld, J
;
Krawitz, P
;
Krüger, U
...
Brownstein Z, Friedman LM, Shahin H, Oron-Karni V, Kol N, Abu Rayyan A, Parzefall T, Lev D, Shalev S, Frydman M, Davidov B, Shohat M, Rahile M, Lieberman S, Levy-Lahad E, Lee MK, Shomron N, King MC, Walsh T, Kanaan M, Avraham KB. Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families. Genome Biol. 2011 Sep 14;12(9):R89. DOI:10.1186/gb-2011-12-9-r89. , 2012
Link:
https://doi.org/10.3205/12dgpp23
RT Journal T1
Phänotypische und genotypische Diagnostik bei non-syndromaler Innenohrschwerhörigkeit
UL https://suche.suub.uni-bremen.de/peid=base-ftgms:oai:oai-gms.dimdi.de:GM12dgpp23&Exemplar=1&LAN=DE A1 Rosenfeld, J A1 Krawitz, P A1 Krüger, U A1 Appelt, S A1 Hecht, J A1 Timmermann, B A1 Spormann-Lagodzinski, M A1 Gross, M PB German Medical Science GMS Publishing House; Düsseldorf YR 2012 K1 ddc: 610 JF Brownstein Z, Friedman LM, Shahin H, Oron-Karni V, Kol N, Abu Rayyan A, Parzefall T, Lev D, Shalev S, Frydman M, Davidov B, Shohat M, Rahile M, Lieberman S, Levy-Lahad E, Lee MK, Shomron N, King MC, Walsh T, Kanaan M, Avraham KB. Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families. Genome Biol. 2011 Sep 14;12(9):R89. DOI:10.1186/gb-2011-12-9-r89 LK http://dx.doi.org/https://doi.org/10.3205/12dgpp23 DO https://doi.org/10.3205/12dgpp23 SF ELIB - SuUB Bremen
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