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1 Ergebnisse
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Dissecting the genetic complexity of human 6p deletion synd..:
Bogani, Debora
;
Willoughby, Catherine
;
Davies, Jennifer
...
0027-8424. ,
Link:
http://hdl.handle.net/1885/52722
RT Journal T1
Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen
UL https://suche.suub.uni-bremen.de/peid=base-ftanucanberra:oai:openresearch-repository.anu.edu.au:1885_52722&Exemplar=1&LAN=DE A1 Bogani, Debora A1 Willoughby, Catherine A1 Davies, Jennifer A1 Kaur, Kulvinder A1 Mirza, Ghazala A1 Paudyal, Anju A1 Haines, Heather A1 McKeone, Richard A1 Cadman, Matthew A1 Pieles, Guido A1 Schneider, Jurgen E A1 Battacharya, Shoumo A1 Hardy, Andrea A1 Nolan, Patrick A1 Tripodis, Nikos A1 Depew, Michael J A1 Chandrasekara, Ramya A1 Duncan, Gimara A1 Sharpe, Paul T A1 Greenfield, Andy A1 Denny, Paul A1 Brown, Steve D M A1 Ragoussis, Jiannis A1 Arkell, Ruth PB National Academy of Sciences (USA) K1 Keywords: animal experiment K1 animal model K1 anophthalmia K1 article K1 brain malformation K1 chromosome 6p deletion syndrome K1 chromosome deletion K1 congenital heart malformation K1 craniofacial malformation K1 embryo K1 female K1 gene deletion K1 gene locus K1 gene mutation K1 genetic a Anophthalmia K1 ENU mutagenesis K1 Holoprosencephaly JF 0027-8424 LK http://hdl.handle.net/1885/52722 DO http://hdl.handle.net/1885/52722 SF ELIB - SuUB Bremen
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