DELETION Yq DANS LE SYNDROME D'ALCOOLISME FOETAL

Translated title of the contribution: Yq deletion in fetal alcohol syndrome

M. Bozzola, M. S. Scotta, R. Lorini

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

The case of a 10-year-old boy with fetal alcohol syndrome is described. No hormonal abnormality was found. Chromosomal studies from lymphocyte cultures showed a deletion of the heterochromatic portion of the long arm of the Y chromosome: 46,X,del (Y) (pter ← q11). The same chromosomal abnormality was present in his father.

Original languageFrench
Pages (from-to)367-369
Number of pages3
JournalAnnales de Pediatrie
Volume29
Issue number5
Publication statusPublished - 1982

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Fetal Alcohol Spectrum Disorders
Y Chromosome
Fathers
Chromosome Aberrations
Lymphocytes

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Cite this

Bozzola, M., Scotta, M. S., & Lorini, R. (1982). DELETION Yq DANS LE SYNDROME D'ALCOOLISME FOETAL. Annales de Pediatrie, 29(5), 367-369.

DELETION Yq DANS LE SYNDROME D'ALCOOLISME FOETAL. / Bozzola, M.; Scotta, M. S.; Lorini, R.

In: Annales de Pediatrie, Vol. 29, No. 5, 1982, p. 367-369.

Research output: Contribution to journalArticle

Bozzola, M, Scotta, MS & Lorini, R 1982, 'DELETION Yq DANS LE SYNDROME D'ALCOOLISME FOETAL', Annales de Pediatrie, vol. 29, no. 5, pp. 367-369.
Bozzola, M. ; Scotta, M. S. ; Lorini, R. / DELETION Yq DANS LE SYNDROME D'ALCOOLISME FOETAL. In: Annales de Pediatrie. 1982 ; Vol. 29, No. 5. pp. 367-369.
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