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Prenatal diagnosis and genetic analysis of type I and type II thanatophoric dysplasia

Prenatal diagnosis, 2001-02, Vol.21 (2), p.89-95

2001

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Second-trimester diagnosis of complete trisomy 9 associated with abnormal maternal serum screen results, open sacral spina bifida and congenital diaphragmatic hernia, and review of the literature

Prenatal diagnosis, 2004-06, Vol.24 (6), p.455-462

2004

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Prenatal diagnosis, sonographic findings and molecular genetic analysis of a 46,XX/46,XY true hermaphrodite chimera

Prenatal diagnosis, 2005-06, Vol.25 (6), p.502-506

2005

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Prenatal diagnosis of the distal 11q deletion and review of the literature

Prenatal diagnosis, 2004-02, Vol.24 (2), p.130-136

2004

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Prenatal diagnosis of mosaic distal 5p deletion and review of the literature

Prenatal diagnosis, 2004-01, Vol.24 (1), p.50-57

2004

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Contribution of ultrafast magnetic resonance imaging in prenatal diagnosis of sonographically undetected cerebral tuberous sclerosis associated with cardiac rhabdomyomas

Prenatal diagnosis, 2005-06, Vol.25 (6), p.523-524

2005

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Prenatal diagnosis of pure distal 18q deletion

Prenatal diagnosis, 2006-02, Vol.26 (2), p.184-185

2006

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Molecular genetic analysis of the TSC genes in two families with prenatally diagnosed rhabdomyomas

Prenatal diagnosis, 2005-02, Vol.25 (2), p.176-178

2005

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Recurrent fetal pyelectasis in a family with fetuses associated with partial trisomy 10q (10q24.1→qter)

Prenatal diagnosis, 2005-03, Vol.25 (3), p.263-264

2005

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Prenatal diagnosis of an acardiac amorphous twin and the anomalous co-twin in a monoamniotic twin pregnancy

Prenatal diagnosis, 2005-07, Vol.25 (7), p.618-620

2005

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Prenatal diagnosis of partial monosomy 18p(18p11.2→pter) and trisomy 21q(21q22.3→qter) with alobar holoprosencephaly and premaxillary agenesis

Prenatal diagnosis, 2001-05, Vol.21 (5), p.346-350

2001

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Prenatal diagnosis of de novo terminal deletion of chromosome 7q

Prenatal diagnosis, 2003-05, Vol.23 (5), p.375-379

2003

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Perinatal imaging findings of inherited Sotos syndrome

Prenatal diagnosis, 2002-10, Vol.22 (10), p.887-892

2002

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Prenatal diagnosis of the Dandy-Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion

Prenatal diagnosis, 2002-12, Vol.22 (12), p.1063-1066

2002

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The prenatal diagnosis of Pierre-Robin sequence

Prenatal diagnosis, 1999-06, Vol.19 (6), p.567-569

1999

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Prenatal diagnosis of partial trisomy 10q (10q25.3→qter) and partial monosomy 18q (18q23→qter)

Prenatal diagnosis, 2005-11, Vol.25 (11), p.1069-1071

2005

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Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4

Prenatal diagnosis, 2004-01, Vol.24 (1), p.38-44

2004

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Second-trimester sonographic detection of short rib-polydactyly syndrome type II (Majewski) following an abnormal maternal serum biochemical screening result

Prenatal diagnosis, 2003-04, Vol.23 (4), p.353-355

2003

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Prenatal diagnosis of partial trisomy 3p and partial monosomy 11q in a fetus with a Dandy-Walker variant and trigonocephaly

Prenatal diagnosis, 2002-12, Vol.22 (12), p.1112-1113

2002

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Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction

Prenatal diagnosis, 2003-01, Vol.23 (1), p.40-43

2003

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Prenatal diagnosis of Apert syndrome

Prenatal diagnosis, 1998-06, Vol.18 (6), p.621-625

1998

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Prenatal magnetic resonance imaging demonstration of the systemic feeding artery of a pulmonary sequestration associated with in utero regression

Prenatal diagnosis, 2005-08, Vol.25 (8), p.721-723

2005

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Prenatal diagnosis of mosaic 22q11.2 microdeletion

Prenatal diagnosis, 2004-08, Vol.24 (8), p.660-662

2004

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Prenatal diagnosis of de novo proximal interstitial deletion of 9q and review of the literature of uncommon aneuploidies associated with increased nuchal translucency

Prenatal diagnosis, 2005-05, Vol.25 (5), p.383-389

2005

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Prenatal magnetic resonance imaging of Galloway-Mowat syndrome

Prenatal diagnosis, 2005-06, Vol.25 (6), p.525-527

2005

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Prenatal diagnosis and genetic analysis of type I and type II thanatophoric dysplasia

Second-trimester diagnosis of complete trisomy 9 associated with abnormal maternal serum screen results, open sacral spina bifida and congenital diaphragmatic hernia, and review of the literature

Prenatal diagnosis, sonographic findings and molecular genetic analysis of a 46,XX/46,XY true hermaphrodite chimera

Prenatal diagnosis of the distal 11q deletion and review of the literature

Prenatal diagnosis of mosaic distal 5p deletion and review of the literature

Contribution of ultrafast magnetic resonance imaging in prenatal diagnosis of sonographically undetected cerebral tuberous sclerosis associated with cardiac rhabdomyomas

Prenatal diagnosis of pure distal 18q deletion

Molecular genetic analysis of the TSC genes in two families with prenatally diagnosed rhabdomyomas

Recurrent fetal pyelectasis in a family with fetuses associated with partial trisomy 10q (10q24.1→qter)

Prenatal diagnosis of an acardiac amorphous twin and the anomalous co-twin in a monoamniotic twin pregnancy

Prenatal diagnosis of partial monosomy 18p(18p11.2→pter) and trisomy 21q(21q22.3→qter) with alobar holoprosencephaly and premaxillary agenesis

Prenatal diagnosis of de novo terminal deletion of chromosome 7q

Perinatal imaging findings of inherited Sotos syndrome

Prenatal diagnosis of the Dandy-Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion

The prenatal diagnosis of Pierre-Robin sequence

Prenatal diagnosis of partial trisomy 10q (10q25.3→qter) and partial monosomy 18q (18q23→qter)

Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4

Second-trimester sonographic detection of short rib-polydactyly syndrome type II (Majewski) following an abnormal maternal serum biochemical screening result

Prenatal diagnosis of partial trisomy 3p and partial monosomy 11q in a fetus with a Dandy-Walker variant and trigonocephaly

Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction

Prenatal diagnosis of Apert syndrome

Prenatal magnetic resonance imaging demonstration of the systemic feeding artery of a pulmonary sequestration associated with in utero regression

Prenatal diagnosis of mosaic 22q11.2 microdeletion

Prenatal diagnosis of de novo proximal interstitial deletion of 9q and review of the literature of uncommon aneuploidies associated with increased nuchal translucency

Prenatal magnetic resonance imaging of Galloway-Mowat syndrome

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