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S Hadj-Rabia

Showing results (51-60 of 88) with videos related to

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Human Mutation|March 14, 2007
Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locusE Bal, L Baala, C Cluzeau, et al.
The British Journal of Dermatology|February 10, 2015
Paediatric mastocytosis: a systematic review of 1747 casesC Méni, J Bruneau, S Georgin-Lavialle, et al.
Journal of Dental Research|June 8, 2018
Patterns of Dental Agenesis Highlight the Nature of the Causative Mutated GenesB P Fournier, M H Bruneau, S Toupenay, et al.
Journal of Medical Genetics|June 3, 2004
A novel form of syndromic cutis laxa with facial dysmorphism, cleft palate, and mental retardationD Genevieve, C Baumann, C Huber, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 27, 2015
Familial hypochondroplasia and acanthosis nigricans with FGFR3 K650T mutationM A Cossiez Cacard, J Coulombe, P Bernard, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 17, 2009
Prenatal diagnosis of cardiac rhabdomyomas: incidence of associated cerebral lesions of tuberous sclerosis complexJ Saada, S Hadj Rabia, L Fermont, et al.
The British Journal of Dermatology|June 16, 2015
Keratotic follicular plugs with calcifications in Conradi-Hünermann-Happle syndrome: histological, biochemical and genetic testing correlationS Leclerc-Mercier, F Dufernez, S Fraitag, et al.
Clinical Genetics|March 19, 2010
X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findingsF Clauss, N Chassaing, A Smahi, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|October 3, 2020
Immunological and virological profile of children with chilblain-like lesions and SARS-CoV-2L Fertitta, A Welfringer-Morin, A Ouedrani, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|May 26, 2025
Drug management of lichen planus in a paediatric series of 25 patientsE Benassaia, A Welfringer-Morin, N Bellon, et al.
Pageof 9

Showing results (51-60 of 88) with videos related to

Sort By:
Pageof 9
Human Mutation|March 14, 2007
Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locusE Bal, L Baala, C Cluzeau, et al.
The British Journal of Dermatology|February 10, 2015
Paediatric mastocytosis: a systematic review of 1747 casesC Méni, J Bruneau, S Georgin-Lavialle, et al.
Journal of Dental Research|June 8, 2018
Patterns of Dental Agenesis Highlight the Nature of the Causative Mutated GenesB P Fournier, M H Bruneau, S Toupenay, et al.
Journal of Medical Genetics|June 3, 2004
A novel form of syndromic cutis laxa with facial dysmorphism, cleft palate, and mental retardationD Genevieve, C Baumann, C Huber, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 27, 2015
Familial hypochondroplasia and acanthosis nigricans with FGFR3 K650T mutationM A Cossiez Cacard, J Coulombe, P Bernard, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|July 17, 2009
Prenatal diagnosis of cardiac rhabdomyomas: incidence of associated cerebral lesions of tuberous sclerosis complexJ Saada, S Hadj Rabia, L Fermont, et al.
The British Journal of Dermatology|June 16, 2015
Keratotic follicular plugs with calcifications in Conradi-Hünermann-Happle syndrome: histological, biochemical and genetic testing correlationS Leclerc-Mercier, F Dufernez, S Fraitag, et al.
Clinical Genetics|March 19, 2010
X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findingsF Clauss, N Chassaing, A Smahi, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|October 3, 2020
Immunological and virological profile of children with chilblain-like lesions and SARS-CoV-2L Fertitta, A Welfringer-Morin, A Ouedrani, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|May 26, 2025
Drug management of lichen planus in a paediatric series of 25 patientsE Benassaia, A Welfringer-Morin, N Bellon, et al.
Pageof 9