نتائج البحث - Robert Gensure
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A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders حسب Robert Gensure, Outi Mäkitie, Catherine Barclay, Catherine Chan, Steven R. DePalma, Murat Bastepe, H. Abuzahra, Richard Couper, Stefan Mundlos, David Sillence, Leena Ala Kokko, Jonathan G. Seidman, William G. Cole, Harald Jüppner
منشور في 2005Artigo
أدوات البحث:
موضوعات ذات صلة
Medicine
Biology
Calcium
Exon
Gene
Genetics
Internal medicine
Parathyroid hormone
Endocrinology
Allele
Amino acid
Anabolic Agents
Anabolism
Anatomy
Bisphosphonate
Breast cancer
Cancer
Clearance
DNA methylation
Danio
Dosing
GNAS complex locus
Gene expression
Genomic imprinting
Homology (biology)
Hormone
Hormone receptor
Hyperostosis
Imprinting (psychology)
Intron