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Iminophosphanes: Synthesis, Rhodium Complexes, and Ruthenium(II)-Catalyzed Hydration of Nitriles

Organometallics, 2017-03, Vol.36 (5), p.1079-1090

2017

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Rapid detection of chromosomal aneuploidies in uncultured amniocytes by multiplex ligation-dependent probe amplification (MLPA)

Prenatal diagnosis, 2005-11, Vol.25 (11), p.1032-1039

2005

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Correction to Oxidative Addition of Sn–C Bonds on Palladium(0): Identification of Palladium–Stannyl Species and a Facile Synthetic Route to Diphosphinostannylene–Palladium Complexes

Organometallics, 2014-06, Vol.33 (11), p.2914-2918

2014

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Intramolecularly Stabilised Group 10 Metal Stannyl and Stannylene Complexes: Multi-pathway Synthesis and Observation of Platinum-to-Tin Alkyl Transfer

Chemistry : a European journal, 2015-01, Vol.21 (4), p.1765-1779

2015

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Synthesis and Structural Characterization of Lithium and Trimethyltin Complexes of 2,6-Bis(oxazolinyl)phenyl

Organometallics, 2005-02, Vol.24 (4), p.743-749

2005

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Characterization of partial trisomy 9p due to insertional translocation by chromosomal (micro)FISH

Clinical genetics, 2002-12, Vol.62 (6), p.482-487

2002

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Mosaic trisomy (8)(p22 → pter) in a fetus caused by a supernumerary marker chromosome without alphoid sequences

Prenatal diagnosis, 2005-02, Vol.25 (2), p.151-155

2005

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Virilization of the external genitalia and severe mental retardation in a girl with an unbalanced translocation 1;18

European journal of medical genetics, 2006, Vol.49 (1), p.19-27

2006

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Comparative genomic hybridization for cytogenetic evaluation of stillbirth

Obstetrics and gynecology (New York. 1953), 2000-08, Vol.96 (2), p.281-286

2000

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Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniques

Prenatal diagnosis, 2003-09, Vol.23 (9), p.747-751

2003

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Pitfalls in prenatal diagnosis: cytogenetic analysis in amniocytes fails to detect mosaic r(12)

Prenatal diagnosis, 2003-01, Vol.23 (1), p.65-67

2003

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Intramolecularly Stabilised Group10 Metal Stannyl and Stannylene Complexes: Multi-pathway Synthesis and Observation of Platinum-to-Tin Alkyl Transfer

Chemistry : a European journal, 2015-01, Vol.21 (4), p.1765-1779

2015

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Misleading variant chromosome 12 in prenatal diagnosis

Prenatal diagnosis, 2006-06, Vol.26 (6), p.587-588

2006

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Unique mosaicism of structural chromosomal rearrangement: Is chromosome 18 preferentially involved?

American journal of medical genetics. Part A, 2003-05, Vol.119A (1), p.26-31

2003

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Striking facial dysmorphisms and restricted thymic development in a fetus with a 6-megabase deletion of chromosome 14q

Pediatric and developmental pathology, 2005-07, Vol.8 (4), p.497-503

2005

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Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome

Genetic counseling, 2004, Vol.15 (4), p.405

2004

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Palladium(0)-Alkene Bis(triarylphosphine) Complexes as Catalyst Precursors for the Methoxycarbonylation of Styrene

Organometallics, 2005-12, Vol.24 (26), p.6411-6419

2005

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First trimester nuchal anomalies as a prenatal sign of Zellweger syndrome

Prenatal diagnosis, 2000-06, Vol.20 (6), p.520-521

2000

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Paternal duplication of chromosome 5q11.2-5q14 in a male born with craniostenosis, ear tags, kidney dysplasia and several other anomalies

Human genetics, 1993-11, Vol.92 (5), p.481-485

1993

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(Perfluoro)alkylsilyl-Substituted 2-[Bis(4-aryl)phosphino]pyridines: Synthesis and Comparison of Their Palladium Complexes in Methoxycarbonylation of Phenylacetylene in Regular Solvents and Supercritical CO2

Organometallics, 2005-10, Vol.24 (22), p.5299-5310

2005

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Interstitial deletion 11q. Case report and review of the literature

Genetic counseling, 1997, Vol.8 (4), p.335

1997

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Trisomy 8 in chorionic villi-unpredictable results in follow-up

Prenatal diagnosis, 2000-05, Vol.20 (5), p.435-437

2000

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Precarious acrocentric short arm in prenatal diagnosis: no chromosome 14 polymorphism, but trisomy 17p

Genetic counseling, 2000, Vol.11 (3), p.241

2000

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MATERNAL UNIPARENTAL DISOMY FOR CHROMOSOME 22 IN A CHILD WITH GENERALIZED MOSAICISM FOR TRISOMY 22

Prenatal diagnosis, 1997-01, Vol.17 (1), p.81-86

1997

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Paracentric inversion inv(11) (q21q23) in the Netherlands

Human genetics, 1990-06, Vol.85 (1), p.15-20

1990

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Iminophosphanes: Synthesis, Rhodium Complexes, and Ruthenium(II)-Catalyzed Hydration of Nitriles

Rapid detection of chromosomal aneuploidies in uncultured amniocytes by multiplex ligation-dependent probe amplification (MLPA)

Correction to Oxidative Addition of Sn–C Bonds on Palladium(0): Identification of Palladium–Stannyl Species and a Facile Synthetic Route to Diphosphinostannylene–Palladium Complexes

Intramolecularly Stabilised Group 10 Metal Stannyl and Stannylene Complexes: Multi-pathway Synthesis and Observation of Platinum-to-Tin Alkyl Transfer

Synthesis and Structural Characterization of Lithium and Trimethyltin Complexes of 2,6-Bis(oxazolinyl)phenyl

Characterization of partial trisomy 9p due to insertional translocation by chromosomal (micro)FISH

Mosaic trisomy (8)(p22 → pter) in a fetus caused by a supernumerary marker chromosome without alphoid sequences

Virilization of the external genitalia and severe mental retardation in a girl with an unbalanced translocation 1;18

Comparative genomic hybridization for cytogenetic evaluation of stillbirth

Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniques

Pitfalls in prenatal diagnosis: cytogenetic analysis in amniocytes fails to detect mosaic r(12)

Intramolecularly Stabilised Group10 Metal Stannyl and Stannylene Complexes: Multi-pathway Synthesis and Observation of Platinum-to-Tin Alkyl Transfer

Misleading variant chromosome 12 in prenatal diagnosis

Unique mosaicism of structural chromosomal rearrangement: Is chromosome 18 preferentially involved?

Striking facial dysmorphisms and restricted thymic development in a fetus with a 6-megabase deletion of chromosome 14q

Clinical and molecular cytogenetic studies in a case with partial trisomy 12p due to a de novo supernumerary ring chromosome

Palladium(0)-Alkene Bis(triarylphosphine) Complexes as Catalyst Precursors for the Methoxycarbonylation of Styrene

First trimester nuchal anomalies as a prenatal sign of Zellweger syndrome

Paternal duplication of chromosome 5q11.2-5q14 in a male born with craniostenosis, ear tags, kidney dysplasia and several other anomalies

(Perfluoro)alkylsilyl-Substituted 2-[Bis(4-aryl)phosphino]pyridines: Synthesis and Comparison of Their Palladium Complexes in Methoxycarbonylation of Phenylacetylene in Regular Solvents and Supercritical CO2

Interstitial deletion 11q. Case report and review of the literature

Trisomy 8 in chorionic villi-unpredictable results in follow-up

Precarious acrocentric short arm in prenatal diagnosis: no chromosome 14 polymorphism, but trisomy 17p

MATERNAL UNIPARENTAL DISOMY FOR CHROMOSOME 22 IN A CHILD WITH GENERALIZED MOSAICISM FOR TRISOMY 22

Paracentric inversion inv(11) (q21q23) in the Netherlands

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