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P16.05: The influence of chromosomal microarray and NIPT on the diagnostic yield in 6,811 high‐risk pregnancies without ultrasound anomalies

Ultrasound in obstetrics & gynecology, 2017-09, Vol.50 (S1), p.206-206

2017

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SNP array detects chromosome aberrations that we thought do not exist: the first case of an isochromosome Xp (i(X)(p10))

Prenatal diagnosis, 2014-08, Vol.34 (8), p.806-808

2014

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Polyalanine expansion in the ZIC3 gene leading to X-linked heterotaxy with VACTERL association: a new polyalanine disorder?

Journal of medical genetics, 2010-05, Vol.47 (5), p.351-355

2010

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SNP array detects chromosome aberrations that we thought do not exist: the first case of an isochromosome Xp (i(X)(p10)): SNP array detects chromosome aberrations that we thought do not exist

Prenatal diagnosis, 2014-08, Vol.34 (8), p.806-808

2014

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Heparin-induced thrombocytopenia and fat necrosis of the breast

European radiology, 2000-01, Vol.10 (3), p.527-530

2000

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Prenatal ultrasonic diagnosis of obstructive bowel disease: A retrospective analysis

Prenatal diagnosis, 1994-11, Vol.14 (11), p.1035-1041

1994

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Prenatal diagnosis of congenital diaphragmatic hernia: A retrospective analysis of 28 cases

Prenatal diagnosis, 1994-03, Vol.14 (3), p.187-190

1994

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PRENATAL DIAGNOSIS OF FETAL ABDOMINAL WALL DEFECTS: A RETROSPECTIVE ANALYSIS OF 44 CASES

Prenatal diagnosis, 1996-05, Vol.16 (5), p.411-417

1996

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Preterm delivery rate and fetal outcome in structurally affected twin pregnancies: A retrospective matched control study

Prenatal diagnosis, 1993-03, Vol.13 (3), p.155-162

1993

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Prenatal diagnosis of congenital cystic adenomatoid lung malformation: A report of seven cases

Prenatal diagnosis, 1993-01, Vol.13 (1), p.65-71

1993

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Prenatal diagnosis of Klippel—Trenaunay—Weber syndrome: a case report

Ultrasound in obstetrics & gynecology, 1992-09, Vol.2 (5), p.360-363

1992

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Tertiary centre referral of small-for-gestational age pregnancies: A 10-year retrospective analysis

Prenatal diagnosis, 1994-02, Vol.14 (2), p.105-108

1994

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Doppler colour flow mapping of fetal intracerebral arteries in the presence of central nervous system anomalies

Ultrasound in medicine & biology, 1993, Vol.19 (5), p.355-357

1993

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Cordocentesis for rapid karyotyping in fetuses with congenital anomalies or severe IUGR

European journal of obstetrics & gynecology and reproductive biology, 1994-03, Vol.53 (3), p.183-187

1994

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Results of pregnancy termination for foetal congenital or chromosomal disorders or intrauterine foetal death by oral mifepristone and/or intravaginal misoprostol; results of a retrospective study

Nederlands tijdschrift voor geneeskunde, 2007-04, Vol.151 (14), p.815

2007

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Fetal renal artery flow velocity waveforms in the presence of congenital renal tract anomalies

Prenatal diagnosis, 1993-07, Vol.13 (7), p.545-549

1993

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Pre-eclampsia and trisomy 13

European journal of obstetrics & gynecology and reproductive biology, 1995-06, Vol.60 (2), p.201-202

1995

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Doppler colour flow imaging of fetal intracerebral arteries and umbilical artery in the small for gestation; age fetus

BJOG : an international journal of obstetrics and gynaecology, 1994-06, Vol.101 (6), p.504-508

1994

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SNP array detects chromosome aberrations that we thought do not exist: the first case of an isochromosome Xp (i(X)(p10))

Prenatal diagnosis, 2014, Vol.34 (8), p.806-808

2014

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Doppler colour flow imaging of fetal intracerebral arteries and umbilical artery in the small for gestational age fetus

British journal of obstetrics and gynaecology, 1994-06, Vol.101 (6), p.504

1994

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De novo pain and relief of pain after abdominal synthetic mesh implants

Continence (Amsterdam), 2022-12, Vol.4, p.100514, Article 100514

2022

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Polyalanine expansion in the ZIC3 gene leading to X-linked heterotaxy with VACTERL association: a new polyalanine disorder?

Journal of medical genetics, 2010, Vol.47 (5), p.351-355

2010

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P16.05: The influence of chromosomal microarray and NIPT on the diagnostic yield in 6,811 high‐risk pregnancies without ultrasound anomalies

SNP array detects chromosome aberrations that we thought do not exist: the first case of an isochromosome Xp (i(X)(p10))

Polyalanine expansion in the ZIC3 gene leading to X-linked heterotaxy with VACTERL association: a new polyalanine disorder?

SNP array detects chromosome aberrations that we thought do not exist: the first case of an isochromosome Xp (i(X)(p10)): SNP array detects chromosome aberrations that we thought do not exist

Heparin-induced thrombocytopenia and fat necrosis of the breast

Prenatal ultrasonic diagnosis of obstructive bowel disease: A retrospective analysis

Prenatal diagnosis of congenital diaphragmatic hernia: A retrospective analysis of 28 cases

PRENATAL DIAGNOSIS OF FETAL ABDOMINAL WALL DEFECTS: A RETROSPECTIVE ANALYSIS OF 44 CASES

Preterm delivery rate and fetal outcome in structurally affected twin pregnancies: A retrospective matched control study

Prenatal diagnosis of congenital cystic adenomatoid lung malformation: A report of seven cases

Prenatal diagnosis of Klippel—Trenaunay—Weber syndrome: a case report

Tertiary centre referral of small-for-gestational age pregnancies: A 10-year retrospective analysis

Doppler colour flow mapping of fetal intracerebral arteries in the presence of central nervous system anomalies

Cordocentesis for rapid karyotyping in fetuses with congenital anomalies or severe IUGR

Results of pregnancy termination for foetal congenital or chromosomal disorders or intrauterine foetal death by oral mifepristone and/or intravaginal misoprostol; results of a retrospective study

Fetal renal artery flow velocity waveforms in the presence of congenital renal tract anomalies

Pre-eclampsia and trisomy 13

Doppler colour flow imaging of fetal intracerebral arteries and umbilical artery in the small for gestation; age fetus

SNP array detects chromosome aberrations that we thought do not exist: the first case of an isochromosome Xp (i(X)(p10))

Doppler colour flow imaging of fetal intracerebral arteries and umbilical artery in the small for gestational age fetus

De novo pain and relief of pain after abdominal synthetic mesh implants

The influence of SNP‐based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomalies

Polyalanine expansion in the ZIC3 gene leading to X-linked heterotaxy with VACTERL association: a new polyalanine disorder?

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