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1 Ergebnisse
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eP263: A pathogenic deletion at 13q32.1q33.1 presenting wit..:
Tung, Moon Ley
;
Warner, Taylor
;
Bombei, Hannah
..
Genetics in Medicine. 24 (2022) 3 - p. S166-S167 , 2022
Link:
https://doi.org/10.1016/j.gim.2022.01.298
RT Journal T1
eP263: A pathogenic deletion at 13q32.1q33.1 presenting with bilateral sensorineural hearing loss and pigmentation anomalies, mimicking Waardenburg syndrome
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.gim.2022.01.298&Exemplar=1&LAN=DE A1 Tung, Moon Ley A1 Warner, Taylor A1 Bombei, Hannah A1 Safina, Nicole A1 Nagy, Jaime PB Elsevier BV YR 2022 SN 1098-3600 JF Genetics in Medicine VO 24 IS 3 SP S166 OP S167 LK http://dx.doi.org/https://doi.org/10.1016/j.gim.2022.01.298 DO https://doi.org/10.1016/j.gim.2022.01.298 SF ELIB - SuUB Bremen
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