D Molina-Gomes - JoVE Visualize

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Prenatal Diagnosis|February 18, 2006

Partial trisomy 20p resulting from recombination of a maternal pericentric inversion: case report of a prenatal diagnosis by chorionic villus samplingD Molina-Gomes, V Nebout, F Daikha-Dahmane, et al.

Fertility and Sterility|May 8, 2007

Oocyte aneuploidy mechanisms are different in two situations of increased chromosomal risk: older patients and patients with recurrent implantation failure after in vitro fertilizationFrançois Vialard, R Lombroso, M Bergere, et al.

Prenatal Diagnosis|December 24, 2003

Fetal karyotyping after 28 weeks of gestation for late ultrasound findings in a low risk populationC L Drummond, D Molina Gomes, M V Senat, et al.

Journal of Assisted Reproduction and Genetics|February 3, 2009

Preconceptional diagnosis for Robertsonian translocation as an alternative to preimplantation genetic diagnosis in two situations: a pilot studyD Molina Gomes, I Hammoud, M Bailly, et al.

Clinical Case Reports|October 31, 2014

Birth of a boy with isolated short stature after prenatal diagnosis of a Xp22.3 nullosomy due to an inherited t(X;15) (p22.3;p10) translocationE Blondeel, D Molina-Gomes, P Bouhanna, et al.

DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|January 1, 1999

cDNA cloning, tissue distribution and chromosomal localization of the human ID4 geneM Rigolet, T Rich, M S Gross-Morand, et al.

Reproductive Biomedicine Online|August 7, 2008

Stability of aneuploidy rate in polar bodies in two cohorts from the same patientF Vialard, D Molina Gomes, I Hammoud, et al.

Gynecologie, Obstetrique & Fertilite|April 23, 2013

[What does a thorough personality questionnaire, the MMPI-2, tell us about psychological aspects of recurrent miscarriage?]M Jaoul, A Ozon, I Marx de Fossey, et al.

Andrology|September 3, 2013

A genome-wide DNA methylation study in azoospermiaF Ferfouri, F Boitrelle, I Ghout, et al.

Prenatal Diagnosis|December 27, 2005

Mid-trimester hyperechogenic bowel in a fetus of Japanese origin carrying a new mutation of CFTR gene (L548Q)M Yamamoto, D Molina-Gomes, E Girodon-Boulandet, et al.

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Showing results (11-20 of 35) with videos related to

Sort By:

Pageof 4

Prenatal Diagnosis|February 18, 2006

Partial trisomy 20p resulting from recombination of a maternal pericentric inversion: case report of a prenatal diagnosis by chorionic villus samplingD Molina-Gomes, V Nebout, F Daikha-Dahmane, et al.

Fertility and Sterility|May 8, 2007

Oocyte aneuploidy mechanisms are different in two situations of increased chromosomal risk: older patients and patients with recurrent implantation failure after in vitro fertilizationFrançois Vialard, R Lombroso, M Bergere, et al.

Prenatal Diagnosis|December 24, 2003

Fetal karyotyping after 28 weeks of gestation for late ultrasound findings in a low risk populationC L Drummond, D Molina Gomes, M V Senat, et al.

Journal of Assisted Reproduction and Genetics|February 3, 2009

Preconceptional diagnosis for Robertsonian translocation as an alternative to preimplantation genetic diagnosis in two situations: a pilot studyD Molina Gomes, I Hammoud, M Bailly, et al.

Clinical Case Reports|October 31, 2014

Birth of a boy with isolated short stature after prenatal diagnosis of a Xp22.3 nullosomy due to an inherited t(X;15) (p22.3;p10) translocationE Blondeel, D Molina-Gomes, P Bouhanna, et al.

DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|January 1, 1999

cDNA cloning, tissue distribution and chromosomal localization of the human ID4 geneM Rigolet, T Rich, M S Gross-Morand, et al.

Reproductive Biomedicine Online|August 7, 2008

Stability of aneuploidy rate in polar bodies in two cohorts from the same patientF Vialard, D Molina Gomes, I Hammoud, et al.

Gynecologie, Obstetrique & Fertilite|April 23, 2013

[What does a thorough personality questionnaire, the MMPI-2, tell us about psychological aspects of recurrent miscarriage?]M Jaoul, A Ozon, I Marx de Fossey, et al.

Andrology|September 3, 2013

A genome-wide DNA methylation study in azoospermiaF Ferfouri, F Boitrelle, I Ghout, et al.

Prenatal Diagnosis|December 27, 2005

Mid-trimester hyperechogenic bowel in a fetus of Japanese origin carrying a new mutation of CFTR gene (L548Q)M Yamamoto, D Molina-Gomes, E Girodon-Boulandet, et al.

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