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European Journal of Medical Research
|
May 1, 2016
A novel LAMB2 gene mutation associated with a severe phenotype in a neonate with Pierson syndrome
Boutaina Zemrani, François Cachat, Olivier Bonny, et al.
Swiss Medical Weekly
|
January 5, 2010
Molecular autopsy in sudden cardiac death and its implication for families: discussion of the practical, legal and ethical aspects of the multidisciplinary collaboration
Katarzyna Michaud, Florence Fellmann, Hugues Abriel, et al.
BMC Nephrology
|
March 23, 2013
Two new families with hereditary minimal change disease
Hassib Chehade, Francois Cachat, Eric Girardin, et al.
Frontiers in Medicine
|
December 27, 2024
Tuberous sclerosis: a survey in the canton of Vaud, Switzerland
Olivia Hagon-Nicod, Florence Fellmann, Jan Novy, et al.
Fertility and Sterility
|
September 20, 2005
Two fast methods for detection of Y-microdeletions
Isabelle E Aknin-Seifer, Renaud L Touraine, Anne-Karen Faure, et al.
Revue Medicale Suisse
|
March 15, 2014
[Rare vascular diseases]
Luca Calanca, Michèle Depairon, Bruno Tribout, et al.
Revue Medicale Suisse
|
June 23, 2017
[Multidisciplinary cardiogenetic counselling]
Florence Fellmann, Xavier Jeanrenaud, Nicole Sekarski, et al.
American Journal of Human Genetics
|
March 17, 2015
Mutations in NDUFB11, encoding a complex I component of the mitochondrial respiratory chain, cause microphthalmia with linear skin defects syndrome
Vanessa A van Rahden, Erika Fernandez-Vizarra, Malik Alawi, et al.
Human Reproduction (Oxford, England)
|
June 12, 2004
How can the genetic risks of embryo donation be minimized? Proposed guidelines of the French Federation of CECOS (Centre d'Etude et de Conservation des Oeufs et du Sperme)
Patrice Eydoux, François Thepot, Florence Fellmann, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 1, 2010
[R74W;R1070W;D1270N]: a new complex allele responsible for cystic fibrosis
Ana de Prada Merino, Florence Niel Bütschi, Isabelle Bouchardy, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 46) with videos related to
Sort By:
Page
of 5
European Journal of Medical Research
|
May 1, 2016
A novel LAMB2 gene mutation associated with a severe phenotype in a neonate with Pierson syndrome
Boutaina Zemrani, François Cachat, Olivier Bonny, et al.
Swiss Medical Weekly
|
January 5, 2010
Molecular autopsy in sudden cardiac death and its implication for families: discussion of the practical, legal and ethical aspects of the multidisciplinary collaboration
Katarzyna Michaud, Florence Fellmann, Hugues Abriel, et al.
BMC Nephrology
|
March 23, 2013
Two new families with hereditary minimal change disease
Hassib Chehade, Francois Cachat, Eric Girardin, et al.
Frontiers in Medicine
|
December 27, 2024
Tuberous sclerosis: a survey in the canton of Vaud, Switzerland
Olivia Hagon-Nicod, Florence Fellmann, Jan Novy, et al.
Fertility and Sterility
|
September 20, 2005
Two fast methods for detection of Y-microdeletions
Isabelle E Aknin-Seifer, Renaud L Touraine, Anne-Karen Faure, et al.
Revue Medicale Suisse
|
March 15, 2014
[Rare vascular diseases]
Luca Calanca, Michèle Depairon, Bruno Tribout, et al.
Revue Medicale Suisse
|
June 23, 2017
[Multidisciplinary cardiogenetic counselling]
Florence Fellmann, Xavier Jeanrenaud, Nicole Sekarski, et al.
American Journal of Human Genetics
|
March 17, 2015
Mutations in NDUFB11, encoding a complex I component of the mitochondrial respiratory chain, cause microphthalmia with linear skin defects syndrome
Vanessa A van Rahden, Erika Fernandez-Vizarra, Malik Alawi, et al.
Human Reproduction (Oxford, England)
|
June 12, 2004
How can the genetic risks of embryo donation be minimized? Proposed guidelines of the French Federation of CECOS (Centre d'Etude et de Conservation des Oeufs et du Sperme)
Patrice Eydoux, François Thepot, Florence Fellmann, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 1, 2010
[R74W;R1070W;D1270N]: a new complex allele responsible for cystic fibrosis
Ana de Prada Merino, Florence Niel Bütschi, Isabelle Bouchardy, et al.
Page
of 5