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Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans

Human molecular genetics, 2012-04, Vol.21 (7), p.1496-1503

2012

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Sibling risk of pervasive developmental disorder estimated by means of an epidemiologic survey in Nagoya, Japan

Journal of human genetics, 2006-06, Vol.51 (6), p.518-522

2006

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Sibling risk of pervasive developmental disorder estimated by means of an epidemiologic survey in Nagoya, Japan

Journal of human genetics, 2006-06, Vol.51 (6), p.518-522

2006

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Paternal uniparental disomy of chromosome 14 and unique exchange of chromosome 7 in cases of spontaneous abortion

Journal of human genetics, 2005-03, Vol.50 (3), p.112-117

2005

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Prenatal molecular diagnosis of a severe type of L1 syndrome (X-linked hydrocephalus)

Journal of neurosurgery. Pediatrics, 2011-10, Vol.8 (4), p.411

2011

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Maternal uniparental disomy of chromosome 16 in a case of spontaneous abortion

Journal of human genetics, 2004-04, Vol.49 (4), p.177-181

2004

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Parental origin and cell stage of non-disjunction of double trisomy in spontaneous abortion

Congenital anomalies, 2005-03, Vol.45 (1), p.21-25

2005

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Test BR625

Formal methods in system design, 2012-11

2012

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Prenatal molecular diagnosis of a severe type of L1 syndrome (X-linked hydrocephalus): Clinical article

Journal of neurosurgery. Pediatrics, 2011-10, Vol.8 (4), p.411-416

2011

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A Retrospective Evaluation of Maternal Serum Screening for the Detection of Fetal Aneuploidy

Prenatal diagnosis, 1997-09, Vol.17 (9), p.861-866

1997

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First trimester diagnosis of conjoined twins in a triplet pregnancy

European journal of obstetrics & gynecology and reproductive biology, 2006-05, Vol.126 (1), p.132-133

2006

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Establishment of a Polymerase Chain Reaction Method for Detection of Escherichia coli in Amniotic Fluid in Patients with Chorioamnionitis

Fetal diagnosis and therapy, 2008-01, Vol.24 (2), p.132-139

2008

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Evaluation Levels of Cytokines in Amniotic Fluid of Women with Intrauterine Infection in the Early Second Trimester

Fetal diagnosis and therapy, 2006-01, Vol.21 (1), p.45-50

2006

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Searching for Genes for Cleft Lip and/or Palate Based on Breakpoint Analysis of a Balanced Translocation t(9;17)(q32;q12)

The Cleft palate-craniofacial journal, 2009-09, Vol.46 (5), p.532-540

2009

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Three-dimensional ultrasound of dicephalus conjoined twins at 9 weeks of gestation

Prenatal diagnosis, 2005-11, Vol.25 (11), p.1063-1064

2005

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Molecular Genetic Techniques for Prenatal Diagnosis

Congenital anomalies, 1994-09, Vol.34 (3), p.161-174

1994

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Prenatal diagnosis and screening

Nihon rinshō, 2005-12, Vol.63 Suppl 12, p.109

2005

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Reduction of Pleural Effusion by OK-432 in a Fetus Complicated with Congenital Hydrothorax

Fetal diagnosis and therapy, 2004-07, Vol.19 (4), p.327-331

2004

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Multicolour spectral karyotyping for complex chromosomal rearrangements in repeated abortion or congenital anomalies

Prenatal diagnosis, 2001-12, Vol.21 (13), p.1123-1128

2001

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Elevated Aldosterone in Amniotic Fluid and Maternal Blood Has Diagnostic Potential in Pregnancies Complicated with a Fetus of Bartter Syndrome

Fetal diagnosis and therapy, 2005-11, Vol.20 (6), p.481-484

2005

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Diagnosis of fetal rubella infection with reverse transcription and nested polymerase chain reaction: A study of 34 cases diagnosed in fetuses

American journal of obstetrics and gynecology, 1996-02, Vol.174 (2), p.578-582

1996

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Prenatal findings for complete trisomy 9

Prenatal diagnosis, 2003-10, Vol.23 (10), p.866-868

2003

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Antenatal Evaluation of an Encephalocele in a Dizygotic Twin Pregnancy Using Fast Magnetic Resonance Imaging

Fetal diagnosis and therapy, 2003-09, Vol.18 (5), p.338-341

2003

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Pneumomediastinum secondary to hyperemesis gravidarum during early pregnancy

Acta obstetricia et gynecologica Scandinavica, 2001-12, Vol.80 (12), p.1143-1145

2001

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Is Angiotensinogen Gene Polymorphism Associated with Hypertension in Pregnancy?

Hypertension in pregnancy, 1999, Vol.18 (3), p.261-271

1999

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Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans

Sibling risk of pervasive developmental disorder estimated by means of an epidemiologic survey in Nagoya, Japan

Sibling risk of pervasive developmental disorder estimated by means of an epidemiologic survey in Nagoya, Japan

Paternal uniparental disomy of chromosome 14 and unique exchange of chromosome 7 in cases of spontaneous abortion

Prenatal molecular diagnosis of a severe type of L1 syndrome (X-linked hydrocephalus)

Maternal uniparental disomy of chromosome 16 in a case of spontaneous abortion

Parental origin and cell stage of non-disjunction of double trisomy in spontaneous abortion

Test BR625

Prenatal molecular diagnosis of a severe type of L1 syndrome (X-linked hydrocephalus): Clinical article

A Retrospective Evaluation of Maternal Serum Screening for the Detection of Fetal Aneuploidy

First trimester diagnosis of conjoined twins in a triplet pregnancy

Establishment of a Polymerase Chain Reaction Method for Detection of Escherichia coli in Amniotic Fluid in Patients with Chorioamnionitis

Evaluation Levels of Cytokines in Amniotic Fluid of Women with Intrauterine Infection in the Early Second Trimester

Searching for Genes for Cleft Lip and/or Palate Based on Breakpoint Analysis of a Balanced Translocation t(9;17)(q32;q12)

Three-dimensional ultrasound of dicephalus conjoined twins at 9 weeks of gestation

Molecular Genetic Techniques for Prenatal Diagnosis

Prenatal diagnosis and screening

Reduction of Pleural Effusion by OK-432 in a Fetus Complicated with Congenital Hydrothorax

Multicolour spectral karyotyping for complex chromosomal rearrangements in repeated abortion or congenital anomalies

Elevated Aldosterone in Amniotic Fluid and Maternal Blood Has Diagnostic Potential in Pregnancies Complicated with a Fetus of Bartter Syndrome

Diagnosis of fetal rubella infection with reverse transcription and nested polymerase chain reaction: A study of 34 cases diagnosed in fetuses

Prenatal findings for complete trisomy 9

Antenatal Evaluation of an Encephalocele in a Dizygotic Twin Pregnancy Using Fast Magnetic Resonance Imaging

Pneumomediastinum secondary to hyperemesis gravidarum during early pregnancy

Is Angiotensinogen Gene Polymorphism Associated with Hypertension in Pregnancy?

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