Clinical and molecular studies in fragile X patients with a Prader-Willi-like phenotype [3]

G. Gillessen-Kaesbach*, B. Horsthemke

*Corresponding author for this work
9 Citations (Scopus)
Original languageEnglish
JournalJournal of Medical Genetics
Volume31
Issue number3
Pages (from-to)260-261
Number of pages2
ISSN0022-2593
Publication statusPublished - 1994

Research Areas and Centers

  • Research Area: Medical Genetics

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