Associated Papers
Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era.
Fang Q et al.
Endocrine Reviews, 2016
Granulin mutations associated with frontotemporal lobar degeneration and related disorders: an update.
Gijselinck I et al.
Human Mutation, 2008
The maize Single myb histone 1 gene, Smh1, belongs to a novel gene family and encodes a protein that binds telomere DNA repeats in vitro.
Marian CO et al.
Plant Physiology, 2003
Mutation analysis of LMX1B gene in nail-patella syndrome patients.
McIntosh I et al.
American Journal of Human Genetics, 1998
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