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. 1994 Oct;31(10):820. doi: 10.1136/jmg.31.10.820

The Prader-Willi-like phenotype in fragile X patients: a designation facilitating clinical (and molecular) differential diagnosis.

B B De Vries, M F Niermeijer

PMCID: PMC1050136 PMID: 7837263

820

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

Gillessen-Kaesbach G., Horsthemke B. Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype. J Med Genet. 1994 Mar;31(3):260–261. doi: 10.1136/jmg.31.3.260-b. [DOI] [PMC free article] [PubMed] [Google Scholar]
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. Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype. J Med Genet. 1993 Sep;30(9):761–766. doi: 10.1136/jmg.30.9.761. [DOI] [PMC free article] [PubMed] [Google Scholar]

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