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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 syndrome
P 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 cases
N Chassaing, C Cluzeau, E Bal, et al.
Clinical Genetics
|
November 15, 2017
FOXE3 mutations: genotype-phenotype correlations
J 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 features
P 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 OTX2
O Patat, C M A van Ravenswaaij-Arts, J Tantau, et al.
Clinical Genetics
|
October 3, 2009
Novel B3GALTL mutation in Peters-plus Syndrome
J Dassie-Ajdid, A Causse, A Poidvin, et al.
Clinical Genetics
|
March 19, 2010
X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findings
F 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 study
C Tardieu, S Jung, K Niederreither, et al.
Clinical Oral Investigations
|
July 10, 2020
Re-focusing on Agnathia-Otocephaly complex
C Dubucs, N Chassaing, C Sergi, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 33) with videos related to
Sort By:
Page
of 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 syndrome
P 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 cases
N Chassaing, C Cluzeau, E Bal, et al.
Clinical Genetics
|
November 15, 2017
FOXE3 mutations: genotype-phenotype correlations
J 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 features
P 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 OTX2
O Patat, C M A van Ravenswaaij-Arts, J Tantau, et al.
Clinical Genetics
|
October 3, 2009
Novel B3GALTL mutation in Peters-plus Syndrome
J Dassie-Ajdid, A Causse, A Poidvin, et al.
Clinical Genetics
|
March 19, 2010
X-linked and autosomal recessive Hypohidrotic Ectodermal Dysplasia: genotypic-dental phenotypic findings
F 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 study
C Tardieu, S Jung, K Niederreither, et al.
Clinical Oral Investigations
|
July 10, 2020
Re-focusing on Agnathia-Otocephaly complex
C Dubucs, N Chassaing, C Sergi, et al.
Page
of 4