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Johan Robert Helle

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American Journal of Medical Genetics. Part A|March 7, 2013
Hyperphagia, mild developmental delay but apparently no structural brain anomalies in a boy without SOX3 expressionJohan Robert Helle, Tuva Barøy, Doriana Misceo, et al.
Orphanet Journal of Rare Diseases|January 9, 2013
Haploinsufficiency of two histone modifier genes on 6p22.3, ATXN1 and JARID2, is associated with intellectual disabilityTuva Barøy, Doriana Misceo, Petter Strømme, et al.
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Showing results (1-10 of 2) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|March 7, 2013
Hyperphagia, mild developmental delay but apparently no structural brain anomalies in a boy without SOX3 expressionJohan Robert Helle, Tuva Barøy, Doriana Misceo, et al.
Orphanet Journal of Rare Diseases|January 9, 2013
Haploinsufficiency of two histone modifier genes on 6p22.3, ATXN1 and JARID2, is associated with intellectual disabilityTuva Barøy, Doriana Misceo, Petter Strømme, et al.
Pageof 1