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

S Sigaudy

Showing results (1-10 of 48) with videos related to

Pageof 5
Sort By:
Journal of Medical Genetics|April 16, 1998
Costello syndromeN Philip, S Sigaudy
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 24, 1998
About familial interstitial nephritis and retinitis pigmentosaM Tsimaratos, S Sigaudy, N Philip, et al.
American Journal of Medical Genetics|January 11, 1996
Oral-facial-digital syndrome with retinal abnormalities: report of a new caseS Sigaudy, N Philip, C Gire, et al.
Gynecologie, Obstetrique & Fertilite|November 6, 2010
[Fetal dysmorphology: a practical approach in utero]N Philip, E Quarello, G Gorincour, et al.
American Journal of Medical Genetics|May 26, 1998
Renal and retinal involvement in the Sensenbrenner syndromeM Tsimaratos, J Sarles, S Sigaudy, et al.
Gynecologie, Obstetrique, Fertilite & Senologie|September 6, 2017
[How to deal with a fetal head circumference lower than the third percentile?]P Mace, M Milh, N Girard, et al.
Genetic Counseling (Geneva, Switzerland)|April 29, 1998
Neonatal death in Marshall-Smith syndromeC Chatel, F Maazoul, S Sigaudy, et al.
Revue De Laryngologie - Otologie - Rhinologie|April 18, 2013
[Genotype--phenotype correlation limits in sensorineural hearing loss: case report of a three-year-old child with a bilateral cochleovestibular impairment and a molecular variant of the COCH gene]M Montava, S Roman, S Sigaudy, et al.
Clinical Dysmorphology|November 21, 1998
Congenital bowing of the long bones in two fetuses presenting features of Stüve-Wiedemann syndrome and Schwartz-Jampel syndrome type 2S Sigaudy, A Moncla, C Fredouille, et al.
American Journal of Medical Genetics|November 4, 1998
Microcephalic osteodysplastic primordial dwarfism Taybi-Linder type: report of four cases and review of the literatureS Sigaudy, A Toutain, A Moncla, et al.
Pageof 5

Showing results (1-10 of 48) with videos related to

Sort By:
Pageof 5
Journal of Medical Genetics|April 16, 1998
Costello syndromeN Philip, S Sigaudy
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 24, 1998
About familial interstitial nephritis and retinitis pigmentosaM Tsimaratos, S Sigaudy, N Philip, et al.
American Journal of Medical Genetics|January 11, 1996
Oral-facial-digital syndrome with retinal abnormalities: report of a new caseS Sigaudy, N Philip, C Gire, et al.
Gynecologie, Obstetrique & Fertilite|November 6, 2010
[Fetal dysmorphology: a practical approach in utero]N Philip, E Quarello, G Gorincour, et al.
American Journal of Medical Genetics|May 26, 1998
Renal and retinal involvement in the Sensenbrenner syndromeM Tsimaratos, J Sarles, S Sigaudy, et al.
Gynecologie, Obstetrique, Fertilite & Senologie|September 6, 2017
[How to deal with a fetal head circumference lower than the third percentile?]P Mace, M Milh, N Girard, et al.
Genetic Counseling (Geneva, Switzerland)|April 29, 1998
Neonatal death in Marshall-Smith syndromeC Chatel, F Maazoul, S Sigaudy, et al.
Revue De Laryngologie - Otologie - Rhinologie|April 18, 2013
[Genotype--phenotype correlation limits in sensorineural hearing loss: case report of a three-year-old child with a bilateral cochleovestibular impairment and a molecular variant of the COCH gene]M Montava, S Roman, S Sigaudy, et al.
Clinical Dysmorphology|November 21, 1998
Congenital bowing of the long bones in two fetuses presenting features of Stüve-Wiedemann syndrome and Schwartz-Jampel syndrome type 2S Sigaudy, A Moncla, C Fredouille, et al.
American Journal of Medical Genetics|November 4, 1998
Microcephalic osteodysplastic primordial dwarfism Taybi-Linder type: report of four cases and review of the literatureS Sigaudy, A Toutain, A Moncla, et al.
Pageof 5