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 7 (2011), Issue 3 (March)

1. Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome.
   Nat Genet. [Abstract] [Full-text]
2. Mutations in the pre-replication complex cause Meier-Gorlin syndrome.
   Nat Genet. [Abstract] [Full-text]
3. Genetic Defects in Human Pericentrin Are Associated With Severe Insulin Resistance and Diabetes.
   Diabetes, 60(3): 925-935. [Abstract] [Full-text]
4. Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome.
   Nat Genet. [Abstract] [Full-text]
5. Mutations in the pre-replication complex cause Meier-Gorlin syndrome.
   Nat Genet. [Abstract] [Full-text]
6. Genetic Defects in Human Pericentrin Are Associated With Severe Insulin Resistance and Diabetes.
   Diabetes, 60(3): 925-935. [Abstract] [Full-text]
7. Genetic Defects in Human Pericentrin Are Associated With Severe Insulin Resistance and Diabetes.
   Diabetes, 60(3): 925-935. [Abstract] [Full-text]
8. Stimulation of chondrogenesis in ATDC5 chondroprogenitor cells and hypertrophy in mouse by Genkwadaphnin.
   Eur J Pharmacol, 655(1): 9-15. [Abstract] [Full-text]
9. Stimulation of chondrogenesis in ATDC5 chondroprogenitor cells and hypertrophy in mouse by Genkwadaphnin.
   Eur J Pharmacol, 655(1): 9-15. [Abstract] [Full-text]
10. Stimulation of chondrogenesis in ATDC5 chondroprogenitor cells and hypertrophy in mouse by Genkwadaphnin.
    Eur J Pharmacol, 655(1): 9-15. [Abstract] [Full-text]
11. Prevention of intellectual disability through screening for congenital hypothyroidism: how much and at what level?
    Arch Dis Child, 96(4): 374-9. [Abstract] [Full-text]
12. Neuronal migration disorders in microcephalic osteodysplastic primordial dwarfism type I/III.
    Acta Neuropathol, 121(4): 545-54. [Abstract] [Full-text]
13. Neuronal migration disorders in microcephalic osteodysplastic primordial dwarfism type I/III.
    Acta Neuropathol, 121(4): 545-54. [Abstract] [Full-text]
14. Neuronal migration disorders in microcephalic osteodysplastic primordial dwarfism type I/III.
    Acta Neuropathol, 121(4): 545-54. [Abstract] [Full-text]
15. Family caregiver distress with children having rare genetic disorders: a qualitative study involving Russell-Silver Syndrome in Taiwan.
    J Clin Nurs. [Abstract] [Full-text]
16. Family caregiver distress with children having rare genetic disorders: a qualitative study involving Russell-Silver Syndrome in Taiwan.
    J Clin Nurs. [Abstract] [Full-text]
17. Family caregiver distress with children having rare genetic disorders: a qualitative study involving Russell-Silver Syndrome in Taiwan.
    J Clin Nurs. [Abstract] [Full-text]
18. Overexpression of FTL1/DDF1, an AP2 transcription factor, enhances tolerance to cold, drought, and heat stresses in Arabidopsis thaliana.
    Plant Sci, 180(4): 634-41. [Abstract] [Full-text]
19. Constitutive co-suppression of the GA 20-oxidase1 gene in tomato leads to severe defects in vegetative and reproductive development.
    Plant Sci, 180(3): 496-503. [Abstract] [Full-text]
20. Overexpression of FTL1/DDF1, an AP2 transcription factor, enhances tolerance to cold, drought, and heat stresses in Arabidopsis thaliana.
    Plant Sci, 180(4): 634-41. [Abstract] [Full-text]
21. Overexpression of FTL1/DDF1, an AP2 transcription factor, enhances tolerance to cold, drought, and heat stresses in Arabidopsis thaliana.
    Plant Sci, 180(4): 634-41. [Abstract] [Full-text]
22. Sulfate in fetal development.
    Semin Cell Dev Biol. [Abstract] [Full-text]
23. Impact of strontium on skeletal deformities in Baltic cod (Gadus morhua callaris L.).
    Chemosphere, 83(4): 486-91. [Abstract] [Full-text]
24. Impact of strontium on skeletal deformities in Baltic cod (Gadus morhua callaris L.).
    Chemosphere, 83(4): 486-91. [Abstract] [Full-text]
25. Impact of strontium on skeletal deformities in Baltic cod (Gadus morhua callaris L.).
    Chemosphere, 83(4): 486-91. [Abstract] [Full-text]
26. Mutations in ORC1, encoding the largest subunit of the origin recognition complex, cause microcephalic primordial dwarfism resembling Meier-Gorlin syndrome.
    Nat Genet, 43(4): 350-5. [Abstract] [Full-text]
27. Mutations in the pre-replication complex cause Meier-Gorlin syndrome.
    Nat Genet, 43(4): 356-9. [Abstract] [Full-text]

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