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1 Ergebnisse
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A Novel 13q12 Microdeletion Associated with Familial Syndro..:
Jasmine Y. Serpen
;
William Presley
;
Adelyn Beil
...
Human Genomics and Genetic Diseases. , 2023
Link:
https://doi.org/10.3390/genes14051034
RT Journal T1
A Novel 13q12 Microdeletion Associated with Familial Syndromic Corneal Opacification
UL https://suche.suub.uni-bremen.de/peid=base-ftmdpi:oai:mdpi.com:_2073-4425_14_5_1034_&Exemplar=1&LAN=DE A1 Jasmine Y. Serpen A1 William Presley A1 Adelyn Beil A1 Stephen T. Armenti A1 Kayla Johnson A1 Shahzad I. Mian A1 Jeffrey W. Innis A1 Lev Prasov PB Multidisciplinary Digital Publishing Institute YR 2023 K1 13q12.11 microdeletion K1 corneal opacification K1 tracheomalacia K1 laryngomalacia K1 hearing loss K1 XPO4 K1 LATS2 K1 ZDHHC20 K1 IFT88 K1 SMAD signaling JF Human Genomics and Genetic Diseases LK http://dx.doi.org/https://doi.org/10.3390/genes14051034 DO https://doi.org/10.3390/genes14051034 SF ELIB - SuUB Bremen
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