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H Robin

Showing results (121-130 of 297) with videos related to

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American Journal of Medical Genetics. Part A|December 7, 2013
Classic phenotype of Coffin-Lowry syndrome in a female with stimulus-induced drop episodes and a genotype with preserved N-terminal kinase domainKitiwan Rojnueangnit, Julie R Jones, Monica J Basehore, et al.
The Annals of Otology, Rhinology, and Laryngology|August 29, 2000
Epiglottic hypoplasia associated with lacrimo-auriculo-dental-digital syndromeT Azar, J A Scott, J E Arnold, et al.
Broncho-Pneumologie|January 1, 1979
[Correlations between the broncho-alveolar lavage characteristics and the response to the provocation test in bird fancier's lung patients]C Voisin, A B Tonnel, H Robin, et al.
The Journal of Craniofacial Surgery|January 25, 2008
Isolated facial hemihyperplasia: manifestation of Beckwith-Wiedemann syndromeAchara Sathienkijkanchai, Sandra K Prucka, John H Grant, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 10, 1999
Immunoelectron microscopic study of the conjunctiva in cicatricial pemphigoidH Robin, T Hoang-Xuan, O Prisant, et al.
American Journal of Medical Genetics|February 7, 1998
Disorganization in mice and humans and its relation to sporadic birth defectsN H Robin, N Abbadi, S E McCandless, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|June 20, 2015
IRF6 Sequencing in Interrupted CleftingSanmati R Cuddapah, Selma Kominek, John H Grant, et al.
Ophthalmology|October 6, 1997
Epidermolysis bullosa acquisita diagnosed by direct immunoelectron microscopy of the conjunctivaT Hoang-Xuan, H Robin, M Heller, et al.
American Journal of Medical Genetics|August 22, 1997
Duplication 14(q24.3q31) in a father and daughter: delineation of a possible imprinted regionN H Robin, A Harari-Shacham, S Schwartz, et al.
Archives of Otolaryngology--Head & Neck Surgery|September 5, 2001
Pediatric otolaryngologists' knowledge and understanding of genetic testing for deafnessN H Robin, C Dietz, J E Arnold, et al.
Pageof 30

Showing results (121-130 of 297) with videos related to

Sort By:
Pageof 30
American Journal of Medical Genetics. Part A|December 7, 2013
Classic phenotype of Coffin-Lowry syndrome in a female with stimulus-induced drop episodes and a genotype with preserved N-terminal kinase domainKitiwan Rojnueangnit, Julie R Jones, Monica J Basehore, et al.
The Annals of Otology, Rhinology, and Laryngology|August 29, 2000
Epiglottic hypoplasia associated with lacrimo-auriculo-dental-digital syndromeT Azar, J A Scott, J E Arnold, et al.
Broncho-Pneumologie|January 1, 1979
[Correlations between the broncho-alveolar lavage characteristics and the response to the provocation test in bird fancier's lung patients]C Voisin, A B Tonnel, H Robin, et al.
The Journal of Craniofacial Surgery|January 25, 2008
Isolated facial hemihyperplasia: manifestation of Beckwith-Wiedemann syndromeAchara Sathienkijkanchai, Sandra K Prucka, John H Grant, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|February 10, 1999
Immunoelectron microscopic study of the conjunctiva in cicatricial pemphigoidH Robin, T Hoang-Xuan, O Prisant, et al.
American Journal of Medical Genetics|February 7, 1998
Disorganization in mice and humans and its relation to sporadic birth defectsN H Robin, N Abbadi, S E McCandless, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|June 20, 2015
IRF6 Sequencing in Interrupted CleftingSanmati R Cuddapah, Selma Kominek, John H Grant, et al.
Ophthalmology|October 6, 1997
Epidermolysis bullosa acquisita diagnosed by direct immunoelectron microscopy of the conjunctivaT Hoang-Xuan, H Robin, M Heller, et al.
American Journal of Medical Genetics|August 22, 1997
Duplication 14(q24.3q31) in a father and daughter: delineation of a possible imprinted regionN H Robin, A Harari-Shacham, S Schwartz, et al.
Archives of Otolaryngology--Head & Neck Surgery|September 5, 2001
Pediatric otolaryngologists' knowledge and understanding of genetic testing for deafnessN H Robin, C Dietz, J E Arnold, et al.
Pageof 30