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Other genetic syndromes:
Brancio-otic dysplasia, collagen defects, skeletal dysplasias, growth abnormalities, acromegaloidism

Articles

SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes.  (PDF)

Bone mineral density and fractures in Turner syndrome.  (PDF)

A syndrome of overgrowth and acromegaloidism with normal growth hormone secretion is associated with chromosome 11 pericentric inversion.

Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST).  (PDF)

Premature adrenal cortical dysfunction in mandibuloacral dysplasia: a progeroid-like syndrome.  (PDF)