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N Chassaing

Showing results (21-30 of 33) with videos related to

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Journal of Medical Genetics|April 16, 2002
Molecular characterisation of a ring chromosome 22 in a patient with severe language delay: a contribution to the refinement of the subtelomeric 22q deletion syndromeP De Mas, N Chassaing, Y Chaix, et al.
Annales De Dermatologie Et De Venereologie|October 21, 2006
[Increased haemoglobin A2 levels in pseudoxanthoma elasticum]L Martin, S Pissard, P Blanc, et al.
The British Journal of Dermatology|March 13, 2010
Mutations in EDARADD account for a small proportion of hypohidrotic ectodermal dysplasia casesN Chassaing, C Cluzeau, E Bal, et al.
Clinical Genetics|November 15, 2017
FOXE3 mutations: genotype-phenotype correlationsJ Plaisancié, N K Ragge, H Dollfus, et al.
European Journal of Medical Genetics|November 5, 2017
4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular featuresP Vande Perre, C Zazo Seco, O Patat, et al.
Molecular Syndromology|October 30, 2013
Otocephaly-Dysgnathia Complex: Description of Four Cases and Confirmation of the Role of OTX2O Patat, C M A van Ravenswaaij-Arts, J Tantau, et al.
Clinical Genetics|October 3, 2009
Novel B3GALTL mutation in Peters-plus SyndromeJ Dassie-Ajdid, A Causse, A Poidvin, 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.
Clinical Genetics|January 21, 2017
Dental and extra-oral clinical features in 41 patients with WNT10A gene mutations: A multicentric genotype-phenotype studyC Tardieu, S Jung, K Niederreither, et al.
Clinical Oral Investigations|July 10, 2020
Re-focusing on Agnathia-Otocephaly complexC Dubucs, N Chassaing, C Sergi, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Journal of Medical Genetics|April 16, 2002
Molecular characterisation of a ring chromosome 22 in a patient with severe language delay: a contribution to the refinement of the subtelomeric 22q deletion syndromeP De Mas, N Chassaing, Y Chaix, et al.
Annales De Dermatologie Et De Venereologie|October 21, 2006
[Increased haemoglobin A2 levels in pseudoxanthoma elasticum]L Martin, S Pissard, P Blanc, et al.
The British Journal of Dermatology|March 13, 2010
Mutations in EDARADD account for a small proportion of hypohidrotic ectodermal dysplasia casesN Chassaing, C Cluzeau, E Bal, et al.
Clinical Genetics|November 15, 2017
FOXE3 mutations: genotype-phenotype correlationsJ Plaisancié, N K Ragge, H Dollfus, et al.
European Journal of Medical Genetics|November 5, 2017
4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular featuresP Vande Perre, C Zazo Seco, O Patat, et al.
Molecular Syndromology|October 30, 2013
Otocephaly-Dysgnathia Complex: Description of Four Cases and Confirmation of the Role of OTX2O Patat, C M A van Ravenswaaij-Arts, J Tantau, et al.
Clinical Genetics|October 3, 2009
Novel B3GALTL mutation in Peters-plus SyndromeJ Dassie-Ajdid, A Causse, A Poidvin, 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.
Clinical Genetics|January 21, 2017
Dental and extra-oral clinical features in 41 patients with WNT10A gene mutations: A multicentric genotype-phenotype studyC Tardieu, S Jung, K Niederreither, et al.
Clinical Oral Investigations|July 10, 2020
Re-focusing on Agnathia-Otocephaly complexC Dubucs, N Chassaing, C Sergi, et al.
Pageof 4