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American Journal of Medical Genetics
|
December 18, 2001
Perinatal hypophosphatasia: radiology, pathology and molecular biology studies in a family harboring a splicing mutation (648+1A) and a novel missense mutation (N400S) in the tissue-nonspecific alkaline phosphatase (TNSALP) gene
C Sergi, E Mornet, J Troeger, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases
|
July 3, 2014
Recurrent neuroendocrine adenoma of the middle ear: a case report
Y Gobel, C La Croix, E Mornet, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases
|
November 10, 2017
Intralabyrinthine sporadic endolymphatic sac tumour
C Lucas, J-C Leclère, E Mornet, et al.
The Journal of Biological Chemistry
|
December 15, 1989
Characterization of two genes encoding human steroid 11 beta-hydroxylase (P-450(11) beta)
E Mornet, J Dupont, A Vitek, et al.
Clinical Genetics
|
June 18, 1998
The intermediate alleles of the fragile X CGG repeat in patients with mental retardation
E Mornet, C Chateau, B Simon-Bouy, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
September 5, 2008
Neurosurgical aspects of childhood hypophosphatasia
H Collmann, E Mornet, S Gattenlöhner, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases
|
August 24, 2020
Haemangioma of the temporal bone
J-C Roubaud, J-C Leclere, E Mornet, et al.
Bulletin Du Groupement International Pour La Recherche Scientifique En Stomatologie & Odontologie
|
October 19, 2013
Abstracts of the 6th International Alkaline Phosphatase and Hypophosphatasia Symposium, May 16-19, 2012, Huningue, France
A Bloch-Zupan, E Mornet, J-L Millán, et al.
Human Genetics
|
May 8, 2000
Parental origin of the extra chromosome in prenatally diagnosed fetal trisomy 21
F Muller, M Rebiffé, A Taillandier, et al.
Annales D'Oto-Laryngologie Et De Chirurgie Cervico Faciale : Bulletin De La Societe D'Oto-Laryngologie Des Hopitaux De Paris
|
February 19, 2008
[Adult localized congenital cholesteatoma]
E Mornet, C Martins-Carvalho, G Valette, et al.
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of 9
Search research articles
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Showing results (11-20 of 86) with videos related to
Sort By:
Page
of 9
American Journal of Medical Genetics
|
December 18, 2001
Perinatal hypophosphatasia: radiology, pathology and molecular biology studies in a family harboring a splicing mutation (648+1A) and a novel missense mutation (N400S) in the tissue-nonspecific alkaline phosphatase (TNSALP) gene
C Sergi, E Mornet, J Troeger, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases
|
July 3, 2014
Recurrent neuroendocrine adenoma of the middle ear: a case report
Y Gobel, C La Croix, E Mornet, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases
|
November 10, 2017
Intralabyrinthine sporadic endolymphatic sac tumour
C Lucas, J-C Leclère, E Mornet, et al.
The Journal of Biological Chemistry
|
December 15, 1989
Characterization of two genes encoding human steroid 11 beta-hydroxylase (P-450(11) beta)
E Mornet, J Dupont, A Vitek, et al.
Clinical Genetics
|
June 18, 1998
The intermediate alleles of the fragile X CGG repeat in patients with mental retardation
E Mornet, C Chateau, B Simon-Bouy, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
September 5, 2008
Neurosurgical aspects of childhood hypophosphatasia
H Collmann, E Mornet, S Gattenlöhner, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases
|
August 24, 2020
Haemangioma of the temporal bone
J-C Roubaud, J-C Leclere, E Mornet, et al.
Bulletin Du Groupement International Pour La Recherche Scientifique En Stomatologie & Odontologie
|
October 19, 2013
Abstracts of the 6th International Alkaline Phosphatase and Hypophosphatasia Symposium, May 16-19, 2012, Huningue, France
A Bloch-Zupan, E Mornet, J-L Millán, et al.
Human Genetics
|
May 8, 2000
Parental origin of the extra chromosome in prenatally diagnosed fetal trisomy 21
F Muller, M Rebiffé, A Taillandier, et al.
Annales D'Oto-Laryngologie Et De Chirurgie Cervico Faciale : Bulletin De La Societe D'Oto-Laryngologie Des Hopitaux De Paris
|
February 19, 2008
[Adult localized congenital cholesteatoma]
E Mornet, C Martins-Carvalho, G Valette, et al.
Page
of 9