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1 Ergebnisse
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Exome sequencing identifies genetic variants in anophthalmi..:
Li, Jingjing
;
Yang, Wei
;
Wang, Yuejun Jessie
...
qt2g1826fs. , 2022
Link:
https://escholarship.org/uc/item/2g1826fs
RT Journal T1
Exome sequencing identifies genetic variants in anophthalmia and microphthalmia
UL https://suche.suub.uni-bremen.de/peid=base-ftcdlib:oai:escholarship.org:ark:_13030_qt2g1826fs&Exemplar=1&LAN=DE A1 Li, Jingjing A1 Yang, Wei A1 Wang, Yuejun Jessie A1 Ma, Chen A1 Curry, Cynthia J A1 McGoldrick, Daniel A1 Nickerson, Deborah A A1 Chong, Jessica X A1 Blue, Elizabeth E A1 Mullikin, James C A1 Reefhuis, Jennita A1 Nembhard, Wendy N A1 Romitti, Paul A A1 Werler, Martha M A1 Browne, Marilyn L A1 Olshan, Andrew F A1 Finnell, Richard H A1 Feldkamp, Marcia L A1 Pangilinan, Faith A1 Almli, Lynn M A1 Bamshad, Mike J A1 Brody, Lawrence C A1 Jenkins, Mary M A1 Shaw, Gary M A1 Program, NISC Comparative Sequencing A1 Genomics, University of Washington Center for Mendelian A1 Study, Birth Defects Prevention PB eScholarship, University of California YR 2022 K1 Eye Disease and Disorders of Vision K1 Genetics K1 Prevention K1 Pediatric K1 Human Genome K1 Clinical Research K1 Congenital Structural Anomalies K1 Aetiology K1 2.1 Biological and endogenous factors K1 Anophthalmos K1 Exome K1 Humans K1 Infant K1 Microphthalmos K1 Mutation K1 Missense K1 Exome Sequencing K1 congenital abnormalities K1 genetic epidemiology K1 newborn eye abnormalities K1 NISC Comparative Sequencing Program K1 University of Washington Center for Mendelian Genomics K1 National Birth Defects Prevention Study K1 Clinical Sciences JF qt2g1826fs LK http://dx.doi.org/https://escholarship.org/uc/item/2g1826fs DO https://escholarship.org/uc/item/2g1826fs SF ELIB - SuUB Bremen
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