Dwarfism Research Today is a free monthly online journal that collates and summarizes the latest research about Dwarfism, including details on genetics, diet, mental and motor development.

Volume 3 (2007), Issue 6 (June)

1. Seckel syndrome with Morgagni hernia.
   Clin Dysmorphol, 16(3): 209-10. [Abstract] [Full-text]
2. Primary growth hormone (GH) insensitivity and insulin-like growth factor deficiency caused by novel compound heterozygous mutations of the GH receptor gene: genetic and functional studies of simple and compound heterozygous states.
   J Clin Endocrinol Metab, 92(6): 2223-31. [Abstract] [Full-text]
3. Genetic ablation of Rac1 in cartilage results in chondrodysplasia.
   Dev Biol, 306(2): 612-23. [Abstract] [Full-text]
4. The rice OsLOL2 gene encodes a zinc finger protein involved in rice growth and disease resistance.
   Mol Genet Genomics, 278(1): 85-94. [Abstract] [Full-text]
5. Small pituitary size in children with Fanconi anemia.
   Pediatr Blood Cancer, 49(2): 166-70. [Abstract] [Full-text]
6. C-terminal extension of rice glutamate decarboxylase (OsGAD2) functions as an autoinhibitory domain and overexpression of a truncated mutant results in the accumulation of extremely high levels of GABA in plant cells.
   J Exp Bot. [Abstract] [Full-text]
7. Characterization of optical coherence topography findings in Kenny-Caffey syndrome.
   J AAPOS, 11(3): 291-3. [Abstract] [Full-text]
8. Preserved fertility in a non-mosaic Klinefelter patient with a mutation in the fibroblast growth factor receptor 3 gene: case report.
   Hum Reprod, 22(7): 1907-11. [Abstract] [Full-text]
9. A mutation in Tpst2 encoding tyrosylprotein sulfotransferase causes dwarfism associated with hypothyroidism.
   Mol Endocrinol, 21(7): 1713-21. [Abstract] [Full-text]
10. Congenital hypothyroidism, dwarfism, and hearing impairment caused by a missense mutation in the mouse dual oxidase 2 gene, Duox2.
    Mol Endocrinol, 21(7): 1593-602. [Abstract] [Full-text]

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