Silver-Russell phenotype in a patient with pure trisomy 1q32.1-q42.1: further delineation of the pure 1q trisomy syndrome

M M van Haelst, H J F M M Eussen, F Visscher, J L M de Ruijter, S L S Drop, D Lindhout, C H Wouters, L C P Govaerts

Research output: Contribution to journalArticleAcademicpeer-review

20 Citations (Scopus)
Original languageEnglish
Pages (from-to)582-5
Number of pages4
JournalJournal of medical genetics
Volume39
Issue number8
DOIs
Publication statusPublished - Aug 2002

Keywords

  • Abnormalities, Multiple/genetics
  • Adult
  • Chromosomes, Human, Pair 1/genetics
  • Fetal Growth Retardation/genetics
  • Humans
  • In Situ Hybridization, Fluorescence
  • Intellectual Disability/genetics
  • Karyotyping
  • Male
  • Phenotype
  • Syndrome
  • Trisomy/genetics
  • Uniparental Disomy/genetics

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