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Martine Le Merrer

Showing results (31-40 of 113) with videos related to

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Pediatric Radiology|August 6, 2011
Spondyloepimetaphyseal dysplasia, short limb-abnormal calcifications type: progressive radiological findings from fetal age to adolescenceKatya Rozovsky, Jacob Sosna, Martine Le Merrer, et al.
American Journal of Human Genetics|March 5, 2004
Paradoxical NSD1 mutations in Beckwith-Wiedemann syndrome and 11p15 anomalies in Sotos syndromeGeneviève Baujat, Marlène Rio, Sylvie Rossignol, et al.
European Journal of Radiology|July 22, 2014
Fibrous dysplasia and McCune-Albright syndrome: imaging for positive and differential diagnoses, prognosis, and follow-up guidelinesValérie Bousson, Caroline Rey-Jouvin, Jean-Denis Laredo, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 13, 2005
Clinical and molecular overlap in overgrowth syndromesGeneviève Baujat, Marlène Rio, Sylvie Rossignol, et al.
American Journal of Medical Genetics. Part A|June 24, 2004
Clinical and genetic heterogeneity in Desbuquois dysplasiaLaurence Faivre, Martine Le Merrer, Klaus Zerres, et al.
Spine|February 8, 2014
Ischiovertebral dysplasia: a retrospective analysis of 30 consecutive cases pointing out the specifics and risks of the spine managementJean-Charles Aurégan, Thierry Odent, Ryan M Coyle, et al.
Human Mutation|July 28, 2011
Serpentine fibula-polycystic kidney syndrome caused by truncating mutations in NOTCH2Bertrand Isidor, Martine Le Merrer, G Ulrich Exner, et al.
European Journal of Human Genetics : EJHG|August 30, 2007
Czech dysplasia metatarsal type: another type II collagen disorderKristien P Hoornaert, Ivo Marik, Kazimierz Kozlowski, et al.
Best Practice & Research. Clinical Rheumatology|March 11, 2008
Fibrodysplasia ossificans progressivaFrederick S Kaplan, Martine Le Merrer, David L Glaser, et al.
American Journal of Medical Genetics. Part A|May 31, 2013
Acro-osteolysis, keloid like-lesions, distinctive facial features, and overgrowth: two newly recognized patients with premature aging syndrome, Penttinen typeFlore Zufferey, Smaïl Hadj-Rabia, Annachiara De Sandre-Giovannoli, et al.
Pageof 12

Showing results (31-40 of 113) with videos related to

Sort By:
Pageof 12
Pediatric Radiology|August 6, 2011
Spondyloepimetaphyseal dysplasia, short limb-abnormal calcifications type: progressive radiological findings from fetal age to adolescenceKatya Rozovsky, Jacob Sosna, Martine Le Merrer, et al.
American Journal of Human Genetics|March 5, 2004
Paradoxical NSD1 mutations in Beckwith-Wiedemann syndrome and 11p15 anomalies in Sotos syndromeGeneviève Baujat, Marlène Rio, Sylvie Rossignol, et al.
European Journal of Radiology|July 22, 2014
Fibrous dysplasia and McCune-Albright syndrome: imaging for positive and differential diagnoses, prognosis, and follow-up guidelinesValérie Bousson, Caroline Rey-Jouvin, Jean-Denis Laredo, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 13, 2005
Clinical and molecular overlap in overgrowth syndromesGeneviève Baujat, Marlène Rio, Sylvie Rossignol, et al.
American Journal of Medical Genetics. Part A|June 24, 2004
Clinical and genetic heterogeneity in Desbuquois dysplasiaLaurence Faivre, Martine Le Merrer, Klaus Zerres, et al.
Spine|February 8, 2014
Ischiovertebral dysplasia: a retrospective analysis of 30 consecutive cases pointing out the specifics and risks of the spine managementJean-Charles Aurégan, Thierry Odent, Ryan M Coyle, et al.
Human Mutation|July 28, 2011
Serpentine fibula-polycystic kidney syndrome caused by truncating mutations in NOTCH2Bertrand Isidor, Martine Le Merrer, G Ulrich Exner, et al.
European Journal of Human Genetics : EJHG|August 30, 2007
Czech dysplasia metatarsal type: another type II collagen disorderKristien P Hoornaert, Ivo Marik, Kazimierz Kozlowski, et al.
Best Practice & Research. Clinical Rheumatology|March 11, 2008
Fibrodysplasia ossificans progressivaFrederick S Kaplan, Martine Le Merrer, David L Glaser, et al.
American Journal of Medical Genetics. Part A|May 31, 2013
Acro-osteolysis, keloid like-lesions, distinctive facial features, and overgrowth: two newly recognized patients with premature aging syndrome, Penttinen typeFlore Zufferey, Smaïl Hadj-Rabia, Annachiara De Sandre-Giovannoli, et al.
Pageof 12