Segregation analysis of autosomal fragile sites in three families with the fragile X chromosome

C. Barletta, R. M. Ragusa, G. Garofalo, F. Scillato, M. Ruggeri

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

Fragile sites on chromosomes 9, at 9p21, 10, at 10q25 and 12, at 12q24, were found in the lymphocytes of some members of three families during the study for detection of a fragile X chromosome. The sites were found to be heritable and folato-sensitive. The genetic implications of these results are discussed.

Original languageEnglish
Pages (from-to)111-114
Number of pages4
JournalAnnales de Genetique
Volume34
Issue number2
Publication statusPublished - 1991

Fingerprint

Chromosomes, Human, Pair 9
X Chromosome
Lymphocytes

Keywords

  • chromosomes 9, 10, 12, X
  • culture conditions
  • fragile sites

ASJC Scopus subject areas

  • Genetics

Cite this

Segregation analysis of autosomal fragile sites in three families with the fragile X chromosome. / Barletta, C.; Ragusa, R. M.; Garofalo, G.; Scillato, F.; Ruggeri, M.

In: Annales de Genetique, Vol. 34, No. 2, 1991, p. 111-114.

Research output: Contribution to journalArticle

Barletta, C, Ragusa, RM, Garofalo, G, Scillato, F & Ruggeri, M 1991, 'Segregation analysis of autosomal fragile sites in three families with the fragile X chromosome', Annales de Genetique, vol. 34, no. 2, pp. 111-114.
Barletta, C. ; Ragusa, R. M. ; Garofalo, G. ; Scillato, F. ; Ruggeri, M. / Segregation analysis of autosomal fragile sites in three families with the fragile X chromosome. In: Annales de Genetique. 1991 ; Vol. 34, No. 2. pp. 111-114.
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