J N Tsitsiklis|B Van Roy - JoVE Visualize

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IEEE Transactions on Neural Networks|February 6, 2008

Regression methods for pricing complex American-style optionsJ N Tsitsiklis, B Van Roy

Ophtalmologie : Organe De La Societe Francaise D'Ophtalmologie|January 1, 1989

[Hereditary paracentric inversion of chromosome 3]A Neetens, J Dumon, B Van Roy

The Thoracic and Cardiovascular Surgeon|July 23, 2005

Successful extracorporeal lung assistance for overwhelming pneumonia in a patient with undiagnosed full blown aids--a controversial therapy in HIV-patientsH Gutermann, B van Roy, W Meersseman, et al.

Clinical Genetics|November 1, 1993

Application of fluorescence in situ hybridization for early prenatal diagnosis of partial trisomy 6p/monosomy 6q due to a familial pericentric inversionJ G Wauters, P J Bossuyt, L Roelen, et al.

Acta Neurologica Scandinavica. Supplementum|June 30, 2011

Gender differences in risk-taking behaviour in youth with epilepsy: a Norwegian population-based studyK Å Alfstad, J Clench-Aas, B Van Roy, et al.

European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 1, 1987

Antenatal ultrasonographic diagnosis of trisomy 18 (Edwards syndrome)M J Stevens, J Dumon, Y Jacquemyn, et al.

Human Molecular Genetics|October 1, 1992

Segregation of the fragile X mutation from an affected male to his normal daughterP J Willems, B Van Roy, K De Boulle, et al.

Genetic Counseling (Geneva, Switzerland)|January 1, 1992

Expression of the fragile-X in the "premutated"/"non-imprinted" stateR Bilas, D Wilhelm, E Schwinger, et al.

American Journal of Medical Genetics. Supplement|January 1, 1990

Study of the origin of nondisjunction in a family with two cases of Down syndrome using cytogenetic and molecular polymorphismsP Stinissen, B Van Roy, G Van Camp, et al.

Human Genetics|June 1, 1992

Reciprocal translocation between the proximal regions of the long arms of chromosomes 13 and 15 resulting in unbalanced offspring: characterization by fluorescence in situ hybridization and DNA analysisK Mangelschots, B Van Roy, F Speleman, et al.

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Showing results (1-10 of 15) with videos related to

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Pageof 2

IEEE Transactions on Neural Networks|February 6, 2008

Regression methods for pricing complex American-style optionsJ N Tsitsiklis, B Van Roy

Ophtalmologie : Organe De La Societe Francaise D'Ophtalmologie|January 1, 1989

[Hereditary paracentric inversion of chromosome 3]A Neetens, J Dumon, B Van Roy

The Thoracic and Cardiovascular Surgeon|July 23, 2005

Successful extracorporeal lung assistance for overwhelming pneumonia in a patient with undiagnosed full blown aids--a controversial therapy in HIV-patientsH Gutermann, B van Roy, W Meersseman, et al.

Clinical Genetics|November 1, 1993

Application of fluorescence in situ hybridization for early prenatal diagnosis of partial trisomy 6p/monosomy 6q due to a familial pericentric inversionJ G Wauters, P J Bossuyt, L Roelen, et al.

Acta Neurologica Scandinavica. Supplementum|June 30, 2011

Gender differences in risk-taking behaviour in youth with epilepsy: a Norwegian population-based studyK Å Alfstad, J Clench-Aas, B Van Roy, et al.

European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 1, 1987

Antenatal ultrasonographic diagnosis of trisomy 18 (Edwards syndrome)M J Stevens, J Dumon, Y Jacquemyn, et al.

Human Molecular Genetics|October 1, 1992

Segregation of the fragile X mutation from an affected male to his normal daughterP J Willems, B Van Roy, K De Boulle, et al.

Genetic Counseling (Geneva, Switzerland)|January 1, 1992

Expression of the fragile-X in the "premutated"/"non-imprinted" stateR Bilas, D Wilhelm, E Schwinger, et al.

American Journal of Medical Genetics. Supplement|January 1, 1990

Study of the origin of nondisjunction in a family with two cases of Down syndrome using cytogenetic and molecular polymorphismsP Stinissen, B Van Roy, G Van Camp, et al.

Human Genetics|June 1, 1992

Reciprocal translocation between the proximal regions of the long arms of chromosomes 13 and 15 resulting in unbalanced offspring: characterization by fluorescence in situ hybridization and DNA analysisK Mangelschots, B Van Roy, F Speleman, et al.

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