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Homozygous deletion of 21q22.2 in a patient with hypotonia,..:
Hildebrandt, Clara
;
Fulton, Anne
;
Rodan, Lance H.
American Journal of Medical Genetics Part A. 185 (2020) 2 - p. 555-560 , 2020
Link:
https://doi.org/10.1002/ajmg.a.61969
RT Journal T1 <Title>Homozygous deletion of 21q22.2 in a patient with hypotonia, developmental delay, cortical visual impairment, and retinopathy</Title> UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_ajmg.a.61969&Exemplar=1&LAN=DE A1 Hildebrandt, Clara A1 Fulton, Anne A1 Rodan, Lance H. PB Wiley YR 2020 SN 1552-4825 SN 1552-4833 JF American Journal of Medical Genetics Part A VO 185 IS 2 SP 555 OP 560 LK http://dx.doi.org/https://doi.org/10.1002/ajmg.a.61969 DO https://doi.org/10.1002/ajmg.a.61969 SF ELIB - SuUB Bremen
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