Prenatal diagnosis and prenatal imaging of a de novo 46,X,der(Y)t(X;Y)(p22.13;q11.23) leading to functional disomy for the distal end of the X chromosome short arm from Xp22.13 in a phenotypically male fetus with posterior fossa abnormalities.

A. Ghosh; Lucy Higgins; S.A. Larkins; C. Miller; N. Ostojic; W.L. Martin; M. D. Kilby

Prenatal diagnosis and prenatal imaging of a de novo 46,X,der(Y)t(X;Y)(p22.13;q11.23) leading to functional disomy for the distal end of the X chromosome short arm from Xp22.13 in a phenotypically male fetus with posterior fossa abnormalities.

A. Ghosh, Lucy Higgins, S.A. Larkins, C. Miller, N. Ostojic, W.L. Martin, M. D. Kilby

Division of Developmental Biology & Medicine (L5)

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	1068-1071
Number of pages	4
Journal	Prenatal diagnosis
Volume	28
Issue number	11
Publication status	Published - 16 Oct 2008

Cite this

Ghosh, A., Higgins, L., Larkins, S. A., Miller, C., Ostojic, N., Martin, W. L., & Kilby, M. D. (2008). Prenatal diagnosis and prenatal imaging of a de novo 46,X,der(Y)t(X;Y)(p22.13;q11.23) leading to functional disomy for the distal end of the X chromosome short arm from Xp22.13 in a phenotypically male fetus with posterior fossa abnormalities. Prenatal diagnosis, 28(11), 1068-1071.

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title = "Prenatal diagnosis and prenatal imaging of a de novo 46,X,der(Y)t(X;Y)(p22.13;q11.23) leading to functional disomy for the distal end of the X chromosome short arm from Xp22.13 in a phenotypically male fetus with posterior fossa abnormalities.",

author = "A. Ghosh and Lucy Higgins and S.A. Larkins and C. Miller and N. Ostojic and W.L. Martin and Kilby, {M. D.}",

year = "2008",

month = oct,

day = "16",

language = "English",

volume = "28",

pages = "1068--1071",

journal = "Prenatal diagnosis",

issn = "0197-3851",

publisher = "John Wiley & Sons Ltd",

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Ghosh, A, Higgins, L, Larkins, SA, Miller, C, Ostojic, N, Martin, WL & Kilby, MD 2008, 'Prenatal diagnosis and prenatal imaging of a de novo 46,X,der(Y)t(X;Y)(p22.13;q11.23) leading to functional disomy for the distal end of the X chromosome short arm from Xp22.13 in a phenotypically male fetus with posterior fossa abnormalities.', Prenatal diagnosis, vol. 28, no. 11, pp. 1068-1071.

Prenatal diagnosis and prenatal imaging of a de novo 46,X,der(Y)t(X;Y)(p22.13;q11.23) leading to functional disomy for the distal end of the X chromosome short arm from Xp22.13 in a phenotypically male fetus with posterior fossa abnormalities. / Ghosh, A.; Higgins, Lucy; Larkins, S.A. et al.
In: Prenatal diagnosis, Vol. 28, No. 11, 16.10.2008, p. 1068-1071.

Research output: Contribution to journal › Article › peer-review

TY - JOUR

T1 - Prenatal diagnosis and prenatal imaging of a de novo 46,X,der(Y)t(X;Y)(p22.13;q11.23) leading to functional disomy for the distal end of the X chromosome short arm from Xp22.13 in a phenotypically male fetus with posterior fossa abnormalities.

AU - Ghosh, A.

AU - Higgins, Lucy

AU - Larkins, S.A.

AU - Miller, C.

AU - Ostojic, N.

AU - Martin, W.L.

AU - Kilby, M. D.

PY - 2008/10/16

Y1 - 2008/10/16

M3 - Article

SN - 0197-3851

VL - 28

SP - 1068

EP - 1071

JO - Prenatal diagnosis

JF - Prenatal diagnosis

IS - 11

ER -