Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M C Aubry

Showing results (61-70 of 72) with videos related to

Pageof 8
Sort By:
Fetal Diagnosis and Therapy|December 23, 2000
Prenatal diagnosis of sporadic Apert syndrome: a sequential diagnostic approach combining three-dimensional computed tomography and molecular biologyD Mahieu-Caputo, P Sonigo, J Amiel, et al.
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.
Journal of Medical Genetics|March 10, 2001
A new case of exomphalos, short limbs, and macrogonadism syndromeG Viot, E Pannier, L Faivre, 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.
Pageof 8

Showing results (61-70 of 72) with videos related to

Sort By:
Pageof 8
Fetal Diagnosis and Therapy|December 23, 2000
Prenatal diagnosis of sporadic Apert syndrome: a sequential diagnostic approach combining three-dimensional computed tomography and molecular biologyD Mahieu-Caputo, P Sonigo, J Amiel, et al.
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.
Journal of Medical Genetics|March 10, 2001
A new case of exomphalos, short limbs, and macrogonadism syndromeG Viot, E Pannier, L Faivre, 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.
Pageof 8