 | Up a level |
Giri, Dinesh, Vignola, Maria Lillina, Gualtieri, Angelica, Scagliotti, Valeria, McNamara, Paul 
ORCID: 0000-0002-7055-6034, Peak, Matthew ORCID: 0000-0003-1909-3211, Didi, Mohammed, Gaston-Massuet, Carles and Senniappan, Senthil
(2017)
Novel FOXA2 mutation causes Hyperinsulinism, Hypopituitarism with Craniofacial and Endoderm-derived organ abnormalities.
HUMAN MOLECULAR GENETICS, 26 (22).
pp. 4315-4326.
Giri, Dinesh, Rigden, Daniel ORCID: 0000-0002-7565-8937, Didi, Mohammed, Peak, Matthew ORCID: 0000-0003-1909-3211, McNamara, Paul ORCID: 0000-0002-7055-6034 and Senniappan, Senthil
(2017)
Novel compound heterozygous <i>ASXL3</i> mutation causing Bainbridge-ropers like syndrome and primary IGF1 deficiency.
INTERNATIONAL JOURNAL OF PEDIATRIC ENDOCRINOLOGY, 2017 (1).
8-.
Giri, Dinesh, Pintus, Dona, Burnside, Girvan ORCID: 0000-0001-7398-1346, Ghatak, Atrayee, Mehta, Fulya, Paul, Princy and Senniappan, Senthil
(2017)
Treating vitamin D deficiency in children with type I diabetes could improve their glycaemic control.
BMC Research Notes, 10 (1).
465-.