A case of double trisomy in a liveborn infant: 48,XXY,+13

J. B. Mailhes, C. M. Moore, J. J. Gershanik

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Ambiguous genitalia, microcephaly, microphthalmia, hypotelorism, single choanal opening, low set ears, simian creases, Tetralogy of Fallot, bilateral hydronephrosis, and absence of the left ureter characterized an infant that died 1 hour postpartum with the karyotype 48,XXY,+13.

Original languageEnglish (US)
Pages (from-to)147-150
Number of pages4
JournalClinical Genetics
Volume11
Issue number2
StatePublished - 1977
Externally publishedYes

Fingerprint

Microphthalmos
Disorders of Sex Development
Microcephaly
Tetralogy of Fallot
Hydronephrosis
Trisomy
Ureter
Karyotype
Postpartum Period
Ear

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Mailhes, J. B., Moore, C. M., & Gershanik, J. J. (1977). A case of double trisomy in a liveborn infant: 48,XXY,+13. Clinical Genetics, 11(2), 147-150.

A case of double trisomy in a liveborn infant : 48,XXY,+13. / Mailhes, J. B.; Moore, C. M.; Gershanik, J. J.

In: Clinical Genetics, Vol. 11, No. 2, 1977, p. 147-150.

Research output: Contribution to journalArticle

Mailhes, JB, Moore, CM & Gershanik, JJ 1977, 'A case of double trisomy in a liveborn infant: 48,XXY,+13', Clinical Genetics, vol. 11, no. 2, pp. 147-150.
Mailhes JB, Moore CM, Gershanik JJ. A case of double trisomy in a liveborn infant: 48,XXY,+13. Clinical Genetics. 1977;11(2):147-150.
Mailhes, J. B. ; Moore, C. M. ; Gershanik, J. J. / A case of double trisomy in a liveborn infant : 48,XXY,+13. In: Clinical Genetics. 1977 ; Vol. 11, No. 2. pp. 147-150.
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