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

P Labrune

Showing results (81-90 of 122) with videos related to

Pageof 13
Sort By:
Journal of Medical Genetics|January 15, 2003
Deletion in the ABL gene resulting from a meiotic recombination of a maternal (3;22;9)(q22;q12;q34.1) translocationA Aboura, P Labrune, F Perreaux, et al.
American Journal of Medical Genetics. Part A|March 3, 2007
Pure and complete trisomy 18p due to a supernumerary marker chromosome associated with moderate mental retardationP Mabboux, S Brisset, A Aboura, et al.
Gastroenterologie Clinique Et Biologique|August 25, 2001
[Genetic incidence of Gilbert's syndrome in France]B Le Bihan-Levaufre, J Francoual, J Chalas, et al.
Progres En Urologie : Journal De L'Association Francaise D'Urologie Et De La Societe Francaise D'Urologie|March 1, 2013
[Construction and validation of an evaluation tool of sexual health using self-administered questionnaires for an application to metabolic diseases]F Petit, A Hubert-Buron, A Mollet-Boudjemline, et al.
American Journal of Medical Genetics|March 1, 1994
Three new cases of the Schinzel-Giedion syndrome and review of the literatureP Labrune, S Lyonnet, V Zupan, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 29, 2015
[Mild hemophilia A fortuitously discovered during Henoch-Schönlein purpura]B Joly, R d'Oiron, C Desconclois, et al.
American Journal of Human Genetics|June 1, 1991
Single-strand conformation polymorphism for detection of mutations and base substitutions in phenylketonuriaP Labrune, D Melle, F Rey, et al.
Revue Des Maladies Respiratoires|December 29, 2004
[Clinical, haemodynamic and genetic features of familial pulmonary arterial hypertension]B Sztrymf, J Francoual, O Sitbon, et al.
Prenatal Diagnosis|November 25, 2003
Fetal phenotype of Prader-Willi syndrome due to maternal disomy for chromosome 15A Coulomb L'Herminé, A Aboura, S Brisset, et al.
Clinical Genetics|April 10, 2002
Molecular cytogenetic analysis of a Xp21.3-pter deletion in a family with normal and short statureG Tachdjian, F Perreaux, A Aboura, et al.
Pageof 13

Showing results (81-90 of 122) with videos related to

Sort By:
Pageof 13
Journal of Medical Genetics|January 15, 2003
Deletion in the ABL gene resulting from a meiotic recombination of a maternal (3;22;9)(q22;q12;q34.1) translocationA Aboura, P Labrune, F Perreaux, et al.
American Journal of Medical Genetics. Part A|March 3, 2007
Pure and complete trisomy 18p due to a supernumerary marker chromosome associated with moderate mental retardationP Mabboux, S Brisset, A Aboura, et al.
Gastroenterologie Clinique Et Biologique|August 25, 2001
[Genetic incidence of Gilbert's syndrome in France]B Le Bihan-Levaufre, J Francoual, J Chalas, et al.
Progres En Urologie : Journal De L'Association Francaise D'Urologie Et De La Societe Francaise D'Urologie|March 1, 2013
[Construction and validation of an evaluation tool of sexual health using self-administered questionnaires for an application to metabolic diseases]F Petit, A Hubert-Buron, A Mollet-Boudjemline, et al.
American Journal of Medical Genetics|March 1, 1994
Three new cases of the Schinzel-Giedion syndrome and review of the literatureP Labrune, S Lyonnet, V Zupan, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 29, 2015
[Mild hemophilia A fortuitously discovered during Henoch-Schönlein purpura]B Joly, R d'Oiron, C Desconclois, et al.
American Journal of Human Genetics|June 1, 1991
Single-strand conformation polymorphism for detection of mutations and base substitutions in phenylketonuriaP Labrune, D Melle, F Rey, et al.
Revue Des Maladies Respiratoires|December 29, 2004
[Clinical, haemodynamic and genetic features of familial pulmonary arterial hypertension]B Sztrymf, J Francoual, O Sitbon, et al.
Prenatal Diagnosis|November 25, 2003
Fetal phenotype of Prader-Willi syndrome due to maternal disomy for chromosome 15A Coulomb L'Herminé, A Aboura, S Brisset, et al.
Clinical Genetics|April 10, 2002
Molecular cytogenetic analysis of a Xp21.3-pter deletion in a family with normal and short statureG Tachdjian, F Perreaux, A Aboura, et al.
Pageof 13