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The phenotype of 15 cases with rare 8q24.13‐q24.3 deletions..:
Maya, Idit
;
Kahana, Sarit
;
Agmon‐Fishman, Ifaat
...
American Journal of Medical Genetics Part A. 185 (2021) 5 - p. 1461-1467 , 2021
Link:
https://doi.org/10.1002/ajmg.a.62131
RT Journal T1 <Title>The phenotype of 15 cases with rare 8q24.13‐q24.3 deletions–A new syndrome or still an enigma?</Title> UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_ajmg.a.62131&Exemplar=1&LAN=DE A1 Maya, Idit A1 Kahana, Sarit A1 Agmon‐Fishman, Ifaat A1 Klein, Cochava A1 Matar, Reut A1 Berger, Racheli A1 Josefsberg, Sagi Ben Yehoshua A1 Shohat, Mordechai A1 Marom, Daphna A1 Basel‐Salmon, Lina A1 Sagi‐Dain, Lena PB Wiley YR 2021 SN 1552-4825 SN 1552-4833 JF American Journal of Medical Genetics Part A VO 185 IS 5 SP 1461 OP 1467 LK http://dx.doi.org/https://doi.org/10.1002/ajmg.a.62131 DO https://doi.org/10.1002/ajmg.a.62131 SF ELIB - SuUB Bremen
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