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L Mosca

Showing results (131-140 of 139) with videos related to

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Prenatal Diagnosis|June 28, 2011
Refining the critical region for congenital diaphragmatic hernia on chromosome 15q26 from the study of four fetusesA L Mosca, L Pinson, J Andrieux, et al.
Journal of the American College of Cardiology|November 3, 2001
AHA/ACC Guidelines for Preventing Heart Attack and Death in Patients With Atherosclerotic Cardiovascular Disease: 2001 update. A statement for healthcare professionals from the American Heart Association and the American College of CardiologyS C Smith, S N Blair, R O Bonow, et al.
Circulation|September 26, 2001
AHA/ACC Scientific Statement: AHA/ACC guidelines for preventing heart attack and death in patients with atherosclerotic cardiovascular disease: 2001 update: A statement for healthcare professionals from the American Heart Association and the American College of CardiologyS C Smith, S N Blair, R O Bonow, et al.
Clinical Genetics|July 5, 2011
What can we learn from old microdeletion syndromes using array-CGH screening?A L Mosca-Boidron, S Bouquillon, L Faivre, et al.
Molecular Psychiatry|May 12, 2016
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disordersO Mercati, G Huguet, A Danckaert, et al.
Clinical Genetics|March 16, 2013
Molecular characterization of 39 de novo sSMC: contribution to prognosis and genetic counselling, a prospective studyN Marle, D Martinet, A Aboura, et al.
Clinical Genetics|October 21, 2016
Xq28 duplication including MECP2 in six unreported affected females: what can we learn for diagnosis and genetic counselling?S El Chehadeh, R Touraine, F Prieur, et al.
Clinical Genetics|March 20, 2013
Systematic molecular and cytogenetic screening of 100 patients with marfanoid syndromes and intellectual disabilityP Callier, B Aral, N Hanna, et al.
Clinical Genetics|November 20, 2015
Genetic counselling difficulties and ethical implications of incidental findings from array-CGH: a 7-year national surveyM Lefebvre, D Sanlaville, N Marle, et al.
Pageof 14

Showing results (131-140 of 139) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 139 results.
Prenatal Diagnosis|June 28, 2011
Refining the critical region for congenital diaphragmatic hernia on chromosome 15q26 from the study of four fetusesA L Mosca, L Pinson, J Andrieux, et al.
Journal of the American College of Cardiology|November 3, 2001
AHA/ACC Guidelines for Preventing Heart Attack and Death in Patients With Atherosclerotic Cardiovascular Disease: 2001 update. A statement for healthcare professionals from the American Heart Association and the American College of CardiologyS C Smith, S N Blair, R O Bonow, et al.
Circulation|September 26, 2001
AHA/ACC Scientific Statement: AHA/ACC guidelines for preventing heart attack and death in patients with atherosclerotic cardiovascular disease: 2001 update: A statement for healthcare professionals from the American Heart Association and the American College of CardiologyS C Smith, S N Blair, R O Bonow, et al.
Clinical Genetics|July 5, 2011
What can we learn from old microdeletion syndromes using array-CGH screening?A L Mosca-Boidron, S Bouquillon, L Faivre, et al.
Molecular Psychiatry|May 12, 2016
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disordersO Mercati, G Huguet, A Danckaert, et al.
Clinical Genetics|March 16, 2013
Molecular characterization of 39 de novo sSMC: contribution to prognosis and genetic counselling, a prospective studyN Marle, D Martinet, A Aboura, et al.
Clinical Genetics|October 21, 2016
Xq28 duplication including MECP2 in six unreported affected females: what can we learn for diagnosis and genetic counselling?S El Chehadeh, R Touraine, F Prieur, et al.
Clinical Genetics|March 20, 2013
Systematic molecular and cytogenetic screening of 100 patients with marfanoid syndromes and intellectual disabilityP Callier, B Aral, N Hanna, et al.
Clinical Genetics|November 20, 2015
Genetic counselling difficulties and ethical implications of incidental findings from array-CGH: a 7-year national surveyM Lefebvre, D Sanlaville, N Marle, et al.
Pageof 14