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Showing results (31-40 of 60) with videos related to

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Presse Medicale (Paris, France : 1983)|September 13, 1986
[Genetic counseling in cancerology]B Le Marec, E Le Gall, H Journel, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1986
[Anencephaly and diprosopy: 2 cases]H Journel, P Parent, H Leguern, et al.
Pediatrie|January 1, 1989
[Congenital diaphragmatic hernia with a late disclosure]A Dabadie, J M Schleich, M Roussey, et al.
Annales De Pediatrie|September 1, 1986
[Epilepsy and trisomy 21. Apropos of 27 cases]C Le Berre, H Journel, J Lucas, et al.
American Journal of Medical Genetics|March 8, 2000
Fronto-otopalatodigital osteodysplasia: clinical evidence for a single entity encompassing Melnick-Needles syndrome, otopalatodigital syndrome types 1 and 2, and frontometaphyseal dysplasiaA Verloes, S Lesenfants, M Barr, et al.
Annales De Pediatrie|February 1, 1986
[Wiskott-Alrich syndrome. Apropos of a case]M Roussey, E Le Gall, J L Virelizier, et al.
Journal of Medical Genetics|June 1, 1991
Contribution to carrier detection and genetic counselling in X linked retinoschisisJ Kaplan, A Pelet, H Hentati, et al.
Archives Francaises De Pediatrie|October 1, 1988
[Approaching the gene of mucoviscidosis. New data]C Ferec, J F Morin, P Parent, et al.
Annales De Genetique|January 1, 1985
Trisomy 11p15 and Beckwith-Wiedemann syndrome. Report of two new casesH Journel, J Lucas, C Allaire, et al.
American Journal of Medical Genetics|April 15, 1993
Heterogeneity versus variability in megalocornea-mental retardation (MMR) syndromes: report of new cases and delineation of 4 probable typesA Verloes, H Journel, C Elmer, et al.
Pageof 6

Showing results (31-40 of 60) with videos related to

Sort By:
Pageof 6
Presse Medicale (Paris, France : 1983)|September 13, 1986
[Genetic counseling in cancerology]B Le Marec, E Le Gall, H Journel, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1986
[Anencephaly and diprosopy: 2 cases]H Journel, P Parent, H Leguern, et al.
Pediatrie|January 1, 1989
[Congenital diaphragmatic hernia with a late disclosure]A Dabadie, J M Schleich, M Roussey, et al.
Annales De Pediatrie|September 1, 1986
[Epilepsy and trisomy 21. Apropos of 27 cases]C Le Berre, H Journel, J Lucas, et al.
American Journal of Medical Genetics|March 8, 2000
Fronto-otopalatodigital osteodysplasia: clinical evidence for a single entity encompassing Melnick-Needles syndrome, otopalatodigital syndrome types 1 and 2, and frontometaphyseal dysplasiaA Verloes, S Lesenfants, M Barr, et al.
Annales De Pediatrie|February 1, 1986
[Wiskott-Alrich syndrome. Apropos of a case]M Roussey, E Le Gall, J L Virelizier, et al.
Journal of Medical Genetics|June 1, 1991
Contribution to carrier detection and genetic counselling in X linked retinoschisisJ Kaplan, A Pelet, H Hentati, et al.
Archives Francaises De Pediatrie|October 1, 1988
[Approaching the gene of mucoviscidosis. New data]C Ferec, J F Morin, P Parent, et al.
Annales De Genetique|January 1, 1985
Trisomy 11p15 and Beckwith-Wiedemann syndrome. Report of two new casesH Journel, J Lucas, C Allaire, et al.
American Journal of Medical Genetics|April 15, 1993
Heterogeneity versus variability in megalocornea-mental retardation (MMR) syndromes: report of new cases and delineation of 4 probable typesA Verloes, H Journel, C Elmer, et al.
Pageof 6