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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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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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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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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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(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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Multiphase Systems for the Recycling of Alkoxycarbonylation Catalysts

Advanced synthesis & catalysis, 2006-08, Vol.348 (12-13), p.1447-1458

2006

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Abnormal Chromosome 18 in prenatal diagnosis with holoprosencephaly

Prenatal diagnosis, 1997-09, Vol.17 (9), p.887-888

1997

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Partial monosomy 8p and partial trisomy 8p with moderate mental retardation

Genetic counseling, 1992, Vol.3 (2), p.83

1992

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Two cases of interstitial deletion of the long arm of chromosome 1: del(1)(q21 → q25) and del(1)(q41 → q43)

Clinical genetics, 1985-05, Vol.27 (5), p.515-519

1985

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A third case of de novo partial trisomy 4p

Journal of medical genetics, 1989-05, Vol.26 (5), p.344-345

1989

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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 CO 2

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

2005

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Lightly fluorous [Pd(OAc) 2{P(C 6H 4- p-SiMe 2CH 2CH 2C 6F 13) 3} 2] in the methoxycarbonylation of styrene: Formation, performance and stability of the catalyst system

Journal of molecular catalysis. A, Chemical, 2006-10, Vol.258 (1), p.334-340

2006

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Two cases with different deletions of the long arm of chromosome 7

Journal of medical genetics, 1979-04, Vol.16 (2), p.151-154

1979

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Familial hyperlysinaemia due to L‐lysineα‐ketoglutarate reductase deficiency: Results of attempted treatment

Journal of inherited metabolic disease, 1978-09, Vol.1 (3), p.89-94

1978

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A "normal" girl

Nederlands tijdschrift voor geneeskunde, 1982-06, Vol.126 (25), p.1121

1982

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Roentgencephalometric measurements in trisomy 8 mosaicism: report of three cases

Journal of craniofacial genetics and developmental biology, 1984, Vol.4 (3), p.233

1984

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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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Cerebral gigantism (Sotos syndrome) in two patients with fra(X) chromosomes

American journal of medical genetics, 1986-01, Vol.23 (1-2), p.221-226

1986

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Maternal serum screening for Down syndrome and neural tube defects

Nederlands tijdschrift voor geneeskunde, 1998-02, Vol.142 (8), p.409

1998

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PRENATAL AND POSTNATAL INVESTIGATION OF A CASE WITH MILLER–DIEKER SYNDROME DUE TO A FAMILIAL CRYPTIC TRANSLOCATION t(17;20) (p13.3;q13.3) DETECTED BY FLUORESCENCEIN SITU HYBRIDIZATION

Prenatal diagnosis, 1997-02, Vol.17 (2), p.173-179

1997

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Multiphase Systems for the Recycling of Alkoxycarbonylation Catalysts

ChemInform, 2006-10, Vol.37 (43), p.no-no

2006

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Abnormal chromosome 18 in prenatal diagnosis with holoprosencephaly

Prenatal diagnosis, 1997, Vol.17 (9), p.887-888

1997

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Phosphine in the Venusian Atmosphere: A Strict Upper Limit from SOFIA GREAT Observations

Geophysical research letters, 2022-11, Vol.49 (22), p.n/a

2022

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

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

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

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

(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

Multiphase Systems for the Recycling of Alkoxycarbonylation Catalysts

Abnormal Chromosome 18 in prenatal diagnosis with holoprosencephaly

Partial monosomy 8p and partial trisomy 8p with moderate mental retardation

Two cases of interstitial deletion of the long arm of chromosome 1: del(1)(q21 → q25) and del(1)(q41 → q43)

A third case of de novo partial trisomy 4p

(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 CO 2

Lightly fluorous [Pd(OAc) 2{P(C 6H 4- p-SiMe 2CH 2CH 2C 6F 13) 3} 2] in the methoxycarbonylation of styrene: Formation, performance and stability of the catalyst system

Two cases with different deletions of the long arm of chromosome 7

Familial hyperlysinaemia due to L‐lysineα‐ketoglutarate reductase deficiency: Results of attempted treatment

A "normal" girl

Roentgencephalometric measurements in trisomy 8 mosaicism: report of three cases

Comparative Genomic Hybridization for Cytogenetic Evaluation of Stillbirth

Cerebral gigantism (Sotos syndrome) in two patients with fra(X) chromosomes

Maternal serum screening for Down syndrome and neural tube defects

PRENATAL AND POSTNATAL INVESTIGATION OF A CASE WITH MILLER–DIEKER SYNDROME DUE TO A FAMILIAL CRYPTIC TRANSLOCATION t(17;20) (p13.3;q13.3) DETECTED BY FLUORESCENCEIN SITU HYBRIDIZATION

Multiphase Systems for the Recycling of Alkoxycarbonylation Catalysts

Abnormal chromosome 18 in prenatal diagnosis with holoprosencephaly

Phosphine in the Venusian Atmosphere: A Strict Upper Limit from SOFIA GREAT Observations

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