The prenatal diagnosis of the 48,XXYY syndrome

P. E. Bibbins, R. L. Anderson, J. M. Rary, H. W. Jones

Research output: Contribution to journal › Article

Abstract

A 48,XXYY fetus was diagnosed prenatally in a 34-year old female who was seen at 18.5 weeks of pregnancy for genetic counselling and amniocentesis for advanced maternal age. The pregnancy was terminated, and skin and peripheral blood samples were obtained at the time of delivery. These samples also exhibited the 48,XXYY chromosomal complement.

Original languageEnglish (US)
Pages (from-to)123-125
Number of pages3
JournalPrenatal Diagnosis
Volume2
Issue number2
StatePublished - 1982
Externally publishedYes

Fingerprint

Klinefelter Syndrome
Prenatal Diagnosis
Pregnancy
Amniocentesis
Genetic Counseling
Maternal Age
Fetus
Skin

ASJC Scopus subject areas

  • Genetics(clinical)
  • Obstetrics and Gynecology

Cite this

Bibbins, P. E., Anderson, R. L., Rary, J. M., & Jones, H. W. (1982). The prenatal diagnosis of the 48,XXYY syndrome. Prenatal Diagnosis, 2(2), 123-125.

The prenatal diagnosis of the 48,XXYY syndrome. / Bibbins, P. E.; Anderson, R. L.; Rary, J. M.; Jones, H. W.

In: Prenatal Diagnosis, Vol. 2, No. 2, 1982, p. 123-125.

Research output: Contribution to journal › Article

Bibbins, PE, Anderson, RL, Rary, JM & Jones, HW 1982, 'The prenatal diagnosis of the 48,XXYY syndrome', Prenatal Diagnosis, vol. 2, no. 2, pp. 123-125.
Bibbins PE, Anderson RL, Rary JM, Jones HW. The prenatal diagnosis of the 48,XXYY syndrome. Prenatal Diagnosis. 1982;2(2):123-125.
Bibbins, P. E. ; Anderson, R. L. ; Rary, J. M. ; Jones, H. W. / The prenatal diagnosis of the 48,XXYY syndrome. In: Prenatal Diagnosis. 1982 ; Vol. 2, No. 2. pp. 123-125.
@article{16fc31ce25054440ad595a8bcde76536,
title = "The prenatal diagnosis of the 48,XXYY syndrome",
abstract = "A 48,XXYY fetus was diagnosed prenatally in a 34-year old female who was seen at 18.5 weeks of pregnancy for genetic counselling and amniocentesis for advanced maternal age. The pregnancy was terminated, and skin and peripheral blood samples were obtained at the time of delivery. These samples also exhibited the 48,XXYY chromosomal complement.",
author = "Bibbins, {P. E.} and Anderson, {R. L.} and Rary, {J. M.} and Jones, {H. W.}",
year = "1982",
language = "English (US)",
volume = "2",
pages = "123--125",
journal = "Prenatal Diagnosis",
issn = "0197-3851",
publisher = "John Wiley and Sons Ltd",
number = "2",

}

TY - JOUR

T1 - The prenatal diagnosis of the 48,XXYY syndrome

AU - Bibbins, P. E.

AU - Anderson, R. L.

AU - Rary, J. M.

AU - Jones, H. W.

PY - 1982

Y1 - 1982

N2 - A 48,XXYY fetus was diagnosed prenatally in a 34-year old female who was seen at 18.5 weeks of pregnancy for genetic counselling and amniocentesis for advanced maternal age. The pregnancy was terminated, and skin and peripheral blood samples were obtained at the time of delivery. These samples also exhibited the 48,XXYY chromosomal complement.

AB - A 48,XXYY fetus was diagnosed prenatally in a 34-year old female who was seen at 18.5 weeks of pregnancy for genetic counselling and amniocentesis for advanced maternal age. The pregnancy was terminated, and skin and peripheral blood samples were obtained at the time of delivery. These samples also exhibited the 48,XXYY chromosomal complement.

UR - http://www.scopus.com/inward/record.url?scp=0020319637&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0020319637&partnerID=8YFLogxK

M3 - Article

C2 - 7145838

AN - SCOPUS:0020319637

VL - 2

SP - 123

EP - 125

JO - Prenatal Diagnosis

JF - Prenatal Diagnosis

SN - 0197-3851

IS - 2

ER -

Access to Document