Fetal ventriculomegaly due to familial submicroscopic terminal 6q deletions

Karin Wadt; Lisa Neerup Jensen; Lise Bjerglund; Majken Søderberg  Lundstrøm; Eva Maria Kirchhoff; Susanne Kjaergaard

doi:10.1002/pd.3981

Fetal ventriculomegaly due to familial submicroscopic terminal 6q deletions

Karin Wadt, Lisa Neerup Jensen, Lise Bjerglund, Majken Søderberg Lundstrøm, Eva Maria Kirchhoff, Susanne Kjaergaard

10 Citationer (Scopus)

Abstract

Submicroscopic terminal 6q deletions are rare. We report on two familial submicroscopic terminal 6q deletions ascertained because of prenatally detected isolated ventriculomegaly and further delineate the variable prenatal and postnatal phenotype. We review published cases of

Originalsprog	Engelsk
Tidsskrift	Prenatal Diagnosis
Vol/bind	32
Udgave nummer	12
Sider (fra-til)	1212-1217
Antal sider	6
ISSN	0197-3851
DOI	https://doi.org/10.1002/pd.3981
Status	Udgivet - 2012

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10.1002/pd.3981

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title = "Fetal ventriculomegaly due to familial submicroscopic terminal 6q deletions",

abstract = "Submicroscopic terminal 6q deletions are rare. We report on two familial submicroscopic terminal 6q deletions ascertained because of prenatally detected isolated ventriculomegaly and further delineate the variable prenatal and postnatal phenotype. We review published cases of ",

author = "Karin Wadt and Jensen, {Lisa Neerup} and Lise Bjerglund and Lundstr{\o}m, {Majken S{\o}derberg} and Kirchhoff, {Eva Maria} and Susanne Kjaergaard",

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AU - Wadt, Karin

AU - Jensen, Lisa Neerup

AU - Bjerglund, Lise

AU - Lundstrøm, Majken Søderberg

AU - Kirchhoff, Eva Maria

AU - Kjaergaard, Susanne

PY - 2012

Y1 - 2012

N2 - Submicroscopic terminal 6q deletions are rare. We report on two familial submicroscopic terminal 6q deletions ascertained because of prenatally detected isolated ventriculomegaly and further delineate the variable prenatal and postnatal phenotype. We review published cases of

AB - Submicroscopic terminal 6q deletions are rare. We report on two familial submicroscopic terminal 6q deletions ascertained because of prenatally detected isolated ventriculomegaly and further delineate the variable prenatal and postnatal phenotype. We review published cases of

U2 - 10.1002/pd.3981

DO - 10.1002/pd.3981

M3 - Journal article

C2 - 23065819

SN - 0197-3851

VL - 32

SP - 1212

EP - 1217

JO - Prenatal Diagnosis

JF - Prenatal Diagnosis

IS - 12

ER -

Fetal ventriculomegaly due to familial submicroscopic terminal 6q deletions

Abstract

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