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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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Malignant Transformation Involving CXXC4 Mutations Identified in a Leukemic Progression Model of Severe Congenital Neutropenia

Cell reports. Medicine, 2020-08, Vol.1 (5), p.100074-100074, Article 100074

2020

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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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Truncated CSF3 receptors induce pro‐inflammatory responses in severe congenital neutropenia

British journal of haematology, 2023-01, Vol.200 (1), p.79-86

2023

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Biomechanical responses of the back of riding horses to water treadmill exercise

The veterinary journal (1997), 2013-12, Vol.198, p.e120-e123

2013

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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 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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PML-controlled responses in severe congenital neutropenia with ELANE-misfolding mutations

Blood advances, 2021-02, Vol.5 (3), p.775-786

2021

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

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

1997

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

Malignant Transformation Involving CXXC4 Mutations Identified in a Leukemic Progression Model of Severe Congenital Neutropenia

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

Truncated CSF3 receptors induce pro‐inflammatory responses in severe congenital neutropenia

Biomechanical responses of the back of riding horses to water treadmill exercise

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

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

PML-controlled responses in severe congenital neutropenia with ELANE-misfolding mutations

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

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

Prenatal detection of complex chromosomal aberrations using advanced molecular cytogenetic techniques

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

(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

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

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

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