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Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
HESX1: a novel gene implicated in a familial form of septo-optic dysplasiaM T Dattani, J P Martinez-Barbera, P Q Thomas, et al.Human Molecular Genetics|January 4, 2001
Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasiaP Q Thomas, M T Dattani, J M Brickman, et al.Journal of Medical Genetics|September 3, 2004
Array comparative genomic hybridisation analysis of boys with X linked hypopituitarism identifies a 3.9 Mb duplicated critical region at Xq27 containing SOX3N M Solomon, S A Ross, T Morgan, et al.Molecular Psychiatry|November 30, 2011
Neurodevelopmental and neuropsychiatric behaviour defects arise from 14-3-3ζ deficiencyP S Cheah, H S Ramshaw, P Q Thomas, et al.Nature Genetics|June 10, 1998
Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouseM T Dattani, J P Martinez-Barbera, P Q Thomas, et al.Pageof 2