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1 Ergebnisse
1
HK1 haemolytic anaemia in association with a neurological p..:
Sasaki, Erina
;
Phelan, Ethna
;
O'Regan, Mary
...
Clinical Genetics. 101 (2021) 1 - p. 142-143 , 2021
Link:
https://doi.org/10.1111/cge.14058
RT Journal T1
HK1 haemolytic anaemia in association with a neurological phenotype and co‐existing CEP290 Meckel–Gruber in a Romani family
UL https://suche.suub.uni-bremen.de/peid=cr-10.1111_cge.14058&Exemplar=1&LAN=DE A1 Sasaki, Erina A1 Phelan, Ethna A1 O'Regan, Mary A1 Kassim, Abdul Halim A1 Miletin, Jan A1 McMahon, Corrina A1 O'Sullivan, Maureen J. A1 Baptista, Julia A1 Lynch, Sally Ann PB Wiley YR 2021 SN 0009-9163 SN 1399-0004 JF Clinical Genetics VO 101 IS 1 SP 142 OP 143 LK http://dx.doi.org/https://doi.org/10.1111/cge.14058 DO https://doi.org/10.1111/cge.14058 SF ELIB - SuUB Bremen
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