M-C Aubry - JoVE Visualize

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Fetal Diagnosis and Therapy|March 27, 2002

Arthrogryposis multiplex congenita and cerebellopontine ischemic lesions in sibs: recurrence of prenatal disruptive brain lesions with different patterns of expression?D Mahieu-Caputo, L J Salomon, M Dommergues, et al.

Journal of Clinical Microbiology|June 28, 2001

Direct detection of Legionella species from bronchoalveolar lavage and open lung biopsy specimens: comparison of LightCycler PCR, in situ hybridization, direct fluorescence antigen detection, and cultureR T Hayden, J R Uhl, X Qian, et al.

Prenatal Diagnosis|November 25, 1998

Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literatureL Faivre, N Morichon-Delvallez, G Viot, et al.

Journal of Medical Genetics|July 7, 2000

Maternal uniparental heterodisomy of chromosome 14: chromosomal mechanism and clinical follow upD Sanlaville, M C Aubry, Y Dumez, et al.

Human Reproduction (Oxford, England)|February 3, 2007

Prenatal diagnosis and normal outcome of a 46,XX/46,XY chimera: a case reportValérie Malan, R Gesny, N Morichon-Delvallez, et al.

Journal of Medical Genetics|August 27, 1998

Cystic fibrosis screening: a fetus with hyperechogenic bowel may be the index caseF Muller, M Dommergues, B Simon-Bouy, et al.

Annals of Oncology : Official Journal of the European Society for Medical Oncology|August 10, 2005

A phase II trial of imatinib (ST1571) in patients with c-kit expressing relapsed small-cell lung cancer: a CALGB and NCCTG studyG K Dy, A A Miller, S J Mandrekar, et al.

Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|September 5, 2012

Three-dimensional helical computed tomography in prenatal diagnosis of fetal skeletal dysplasiaG Macé, P Sonigo, V Cormier-Daire, et al.

Oncogene|September 17, 2013

ASCL1 and RET expression defines a clinically relevant subgroup of lung adenocarcinoma characterized by neuroendocrine differentiationF Kosari, C M Ida, M-C Aubry, et al.

Journal of Medical Genetics|September 20, 2005

Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human developmentD Sanlaville, H C Etchevers, M Gonzales, et al.

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Showing results (51-60 of 60) with videos related to

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You have reached the last page of results.This site can display upto 60 results.

Fetal Diagnosis and Therapy|March 27, 2002

Journal of Clinical Microbiology|June 28, 2001

Prenatal Diagnosis|November 25, 1998

Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literatureL Faivre, N Morichon-Delvallez, G Viot, et al.

Journal of Medical Genetics|July 7, 2000

Maternal uniparental heterodisomy of chromosome 14: chromosomal mechanism and clinical follow upD Sanlaville, M C Aubry, Y Dumez, et al.

Human Reproduction (Oxford, England)|February 3, 2007

Prenatal diagnosis and normal outcome of a 46,XX/46,XY chimera: a case reportValérie Malan, R Gesny, N Morichon-Delvallez, et al.

Journal of Medical Genetics|August 27, 1998

Cystic fibrosis screening: a fetus with hyperechogenic bowel may be the index caseF Muller, M Dommergues, B Simon-Bouy, et al.

Annals of Oncology : Official Journal of the European Society for Medical Oncology|August 10, 2005

A phase II trial of imatinib (ST1571) in patients with c-kit expressing relapsed small-cell lung cancer: a CALGB and NCCTG studyG K Dy, A A Miller, S J Mandrekar, et al.

Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|September 5, 2012

Three-dimensional helical computed tomography in prenatal diagnosis of fetal skeletal dysplasiaG Macé, P Sonigo, V Cormier-Daire, et al.

Oncogene|September 17, 2013

ASCL1 and RET expression defines a clinically relevant subgroup of lung adenocarcinoma characterized by neuroendocrine differentiationF Kosari, C M Ida, M-C Aubry, et al.

Journal of Medical Genetics|September 20, 2005

Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human developmentD Sanlaville, H C Etchevers, M Gonzales, et al.

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