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1 Ergebnisse
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Null variants and deletions in BRWD3 cause an X‐linked synd..:
Ostrowski, Philip J.
;
Zachariou, Anna
;
Loveday, Chey
...
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 181 (2019) 4 - p. 638-643 , 2019
Link:
https://doi.org/10.1002/ajmg.c.31750
RT Journal T1
Null variants and deletions in BRWD3 cause an X‐linked syndrome of mild–moderate intellectual disability, macrocephaly, and obesity: A series of 17 patients
UL https://suche.suub.uni-bremen.de/peid=cr-10.1002_ajmg.c.31750&Exemplar=1&LAN=DE A1 Ostrowski, Philip J. A1 Zachariou, Anna A1 Loveday, Chey A1 Baralle, Diana A1 Blair, Edward A1 Douzgou, Sofia A1 Field, Michael A1 Foster, Alison A1 Kyle, Claire A1 Lachlan, Katherine A1 Mansour, Sahar A1 Naik, Swati A1 Rea, Gillian A1 Smithson, Sarah A1 Sznajer, Yves A1 Thompson, Elizabeth A1 Cole, Trevor A1 Tatton‐Brown, Katrina PB Wiley YR 2019 SN 1552-4868 SN 1552-4876 JF American Journal of Medical Genetics Part C: Seminars in Medical Genetics VO 181 IS 4 SP 638 OP 643 LK http://dx.doi.org/https://doi.org/10.1002/ajmg.c.31750 DO https://doi.org/10.1002/ajmg.c.31750 SF ELIB - SuUB Bremen
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