Published in
Wiley, American Journal of Medical Genetics Part C: Seminars in Medical Genetics, 4(181), p. 638-643, 2019
DOI: 10.1002/ajmg.c.31750
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Null variants and deletions in BRWD3 cause an X‐linked syndrome of mild–moderate intellectual disability, macrocephaly, and obesity: A series of 17 patients
Journal article published in 2019 by
Philip J. Ostrowski 
,
Anna Zachariou,
Chey Loveday,
Diana Baralle,
Edward Blair,
Sofia Douzgou,
Michael Field,
Alison Foster ,
Claire Kyle,
Katherine Lachlan,
Sahar Mansour,
Swati Naik,
Gillian Rea,
Sarah Smithson,
Yves Sznajer
and other authors.
,
Anna Zachariou,
Chey Loveday,
Diana Baralle,
Edward Blair,
Sofia Douzgou,
Michael Field,
Alison Foster ,
Claire Kyle,
Katherine Lachlan,
Sahar Mansour,
Swati Naik,
Gillian Rea,
Sarah Smithson,
Yves Sznajer
and other authors.
This paper was not found in any repository, but could be made available legally by the author.
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