Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.
10.1136/jmg.30.9.761
Crossref journal-article
BMJ
Journal of Medical Genetics (239)
Bibliography

de Vries, B. B., Fryns, J. P., Butler, M. G., Canziani, F., Wesby-van Swaay, E., van Hemel, J. O., Oostra, B. A., Halley, D. J., & Niermeijer, M. F. (1993). Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype. Journal of Medical Genetics, 30(9), 761–766.

Authors 9
  1. B B de Vries (first)
  2. J P Fryns (additional)
  3. M G Butler (additional)
  4. F Canziani (additional)
  5. E Wesby-van Swaay (additional)
  6. J O van Hemel (additional)
  7. B A Oostra (additional)
  8. D J Halley (additional)
  9. M F Niermeijer (additional)
References 26 Referenced 74
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Dates
Type When
Created 16 years, 9 months ago (Nov. 10, 2008, 3:23 p.m.)
Deposited 7 months ago (Feb. 2, 2025, 11:36 a.m.)
Indexed 3 months, 1 week ago (May 24, 2025, 4:04 a.m.)
Issued 32 years ago (Sept. 1, 1993)
Published 32 years ago (Sept. 1, 1993)
Published Print 32 years ago (Sept. 1, 1993)
Funders 0

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@article{de_Vries_1993, title={Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype.}, volume={30}, ISSN={1468-6244}, url={http://dx.doi.org/10.1136/jmg.30.9.761}, DOI={10.1136/jmg.30.9.761}, number={9}, journal={Journal of Medical Genetics}, publisher={BMJ}, author={de Vries, B B and Fryns, J P and Butler, M G and Canziani, F and Wesby-van Swaay, E and van Hemel, J O and Oostra, B A and Halley, D J and Niermeijer, M F}, year={1993}, month=sep, pages={761–766} }